Item | Value |
---|---|
geneid | 23149 |
ensemblid | ENSG00000130475.16 |
hgncid | 29002 |
symbol | FCHO1 |
name | FCH and mu domain containing endocytic adaptor 1 |
refseq_nuc | NM_015122.3 |
refseq_prot | NP_055937.1 |
ensembl_nuc | ENST00000596536.6 |
ensembl_prot | ENSP00000470731.1 |
mane_status | MANE Select |
chr | chr19 |
start | 17751477 |
end | 17788561 |
strand | + |
ver | v1.2 |
region | chr19:17751477-17788561 |
region5000 | chr19:17746477-17793561 |
regionname0 | FCHO1_chr19_17751477_17788561 |
regionname5000 | FCHO1_chr19_17746477_17793561 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 889 | 343 | 90 | 78 | 113 | 14 | 46 | 74 | FCHO1_chr19_17746477_17793561 | FCHO1 | MSYFG others(884): Show |
chr19 | 17746477 | 17793561 |
a0002 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | MSYFG others(884): Show |
chr19 | 17746477 | 17793561 |
a0003 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | MSYFG others(884): Show |
chr19 | 17746477 | 17793561 |
a0004 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | MSYFG others(884): Show |
chr19 | 17746477 | 17793561 |
a0005 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | MSYFG others(884): Show |
chr19 | 17746477 | 17793561 |
a0006 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | MSYFG others(884): Show |
chr19 | 17746477 | 17793561 |
a0007 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | MSYFG others(884): Show |
chr19 | 17746477 | 17793561 |
a0008 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | MSYFG others(884): Show |
chr19 | 17746477 | 17793561 |
a0009 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | MSYFG others(884): Show |
chr19 | 17746477 | 17793561 |
a0010 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | MSYFG others(884): Show |
chr19 | 17746477 | 17793561 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2667 | 187 | 48 | 35 | 77 | 5 | 22 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0002 | 1/0 | 2667 | 57 | 21 | 8 | 20 | 0 | 7 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0003 | 0/1 | 2667 | 38 | 5 | 12 | 3 | 6 | 11 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0004 | 0/0 | 2667 | 34 | 7 | 14 | 4 | 3 | 6 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0005 | 0/0 | 2667 | 13 | 0 | 6 | 7 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0006 | 0/0 | 2667 | 5 | 5 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0007 | 0/0 | 2667 | 3 | 2 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0008 | 0/0 | 2667 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0009 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0011 | 0/0 | 2667 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0012 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0016 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0001c0017 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0002c0018 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0003c0021 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0004c0014 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0005c0010 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0006c0013 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0007c0020 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0008c0015 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0009c0019 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 | ||
a0010c0022 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ATGTC others(2662): Show |
chr19 | 17746477 | 17793561 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3208 | 182 | 48 | 34 | 76 | 5 | 19 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0001t0002 | 0/0 | 3208 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0001t0005 | 0/0 | 3208 | 3 | 0 | 1 | 0 | 0 | 2 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0001t0009 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0002t0001 | 1/0 | 3208 | 48 | 16 | 8 | 17 | 0 | 6 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0002t0002 | 0/0 | 3208 | 4 | 3 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0002t0006 | 0/0 | 3208 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0002t0008 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0002t0012 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0002t0013 | 0/0 | 3193 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3188): Show |
chr19 | 17746477 | 17793561 |
a0001c0003t0001 | 0/1 | 3208 | 29 | 5 | 9 | 1 | 4 | 9 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0003t0002 | 0/0 | 3208 | 3 | 0 | 0 | 2 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0003t0004 | 0/0 | 3208 | 4 | 0 | 2 | 0 | 2 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0003t0007 | 0/0 | 3208 | 2 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0004t0001 | 0/0 | 3208 | 2 | 0 | 1 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0004t0002 | 0/0 | 3208 | 22 | 3 | 12 | 1 | 3 | 3 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0004t0003 | 0/0 | 3208 | 8 | 4 | 0 | 2 | 0 | 2 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0004t0010 | 0/0 | 3208 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0004t0011 | 0/0 | 3208 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0005t0001 | 0/0 | 3208 | 13 | 0 | 6 | 7 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0006t0001 | 0/0 | 3208 | 5 | 5 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0007t0002 | 0/0 | 3208 | 2 | 1 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0007t0003 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0008t0003 | 0/0 | 3208 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0009t0002 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0011t0002 | 0/0 | 3208 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0012t0001 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0016t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0001c0017t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0002c0018t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0003c0021t0001 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0004c0014t0001 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0005c0010t0002 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0006c0013t0001 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0007c0020t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0008c0015t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0009c0019t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
a0010c0022t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | ACACA others(3203): Show |
chr19 | 17746477 | 17793561 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0012g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0013g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0304 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0007g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0007g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0010g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0011g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0006t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0006t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0006t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0006t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0006t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0007t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0007t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0007t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0008t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0009t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0011t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0012t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0016t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0017t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0002c0018t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0003c0021t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0004c0014t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0005c0010t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0006c0013t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0007c0020t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0008c0015t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0009c0019t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0010c0022t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | GBR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00140 | hp1 | a0001 | c0004 | t0002 | g0037 | EUR | GBR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0270 | EUR | GBR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0302 | EUR | FIN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00280 | hp2 | a0001 | c0004 | t0002 | g0041 | EUR | FIN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0019 | EUR | FIN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00639 | hp2 | a0001 | c0005 | t0001 | g0136 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00673 | hp2 | a0002 | c0018 | t0001 | g0294 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00733 | hp2 | a0001 | c0008 | t0003 | g0023 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00738 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0312 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01069 | hp2 | a0001 | c0005 | t0001 | g0117 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01070 | hp1 | a0001 | c0004 | t0002 | g0045 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01071 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0239 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01099 | hp2 | a0001 | c0003 | t0004 | g0158 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0159 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0153 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01175 | hp2 | a0001 | c0003 | t0004 | g0163 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0198 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01255 | hp1 | a0001 | c0004 | t0002 | g0038 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0161 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01257 | hp1 | a0001 | c0005 | t0001 | g0108 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01257 | hp2 | a0001 | c0004 | t0002 | g0018 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0160 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01258 | hp2 | a0001 | c0004 | t0002 | g0017 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01346 | hp1 | a0001 | c0004 | t0002 | g0039 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01358 | hp1 | a0001 | c0011 | t0002 | g0063 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01433 | hp2 | a0001 | c0004 | t0002 | g0042 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01516 | hp2 | a0001 | c0003 | t0004 | g0149 | EUR | IBS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01517 | hp1 | a0001 | c0003 | t0004 | g0148 | EUR | IBS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0157 | EUR | IBS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01884 | hp2 | a0001 | c0004 | t0003 | g0020 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01934 | hp1 | a0001 | c0004 | t0001 | g0178 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01943 | hp2 | a0001 | c0005 | t0001 | g0135 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01975 | hp1 | a0001 | c0004 | t0002 | g0004 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01993 | hp1 | a0001 | c0004 | t0010 | g0040 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02004 | hp1 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02004 | hp2 | a0001 | c0004 | t0002 | g0031 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02055 | hp2 | a0001 | c0002 | t0006 | g0185 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02145 | hp2 | a0004 | c0014 | t0001 | g0052 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02148 | hp2 | a0001 | c0004 | t0002 | g0029 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CDX | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02155 | hp2 | a0001 | c0004 | t0001 | g0111 | EAS | CDX | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CDX | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CDX | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02258 | hp1 | a0001 | c0002 | t0006 | g0191 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02258 | hp2 | a0001 | c0007 | t0003 | g0327 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02273 | hp1 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02280 | hp1 | a0001 | c0004 | t0002 | g0026 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02293 | hp2 | a0001 | c0004 | t0002 | g0015 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02300 | hp2 | a0001 | c0003 | t0007 | g0150 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02523 | hp1 | a0001 | c0001 | t0009 | g0216 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02572 | hp1 | a0001 | c0004 | t0003 | g0025 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02602 | hp1 | a0001 | c0004 | t0002 | g0043 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02630 | hp2 | a0001 | c0006 | t0001 | g0182 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0165 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02698 | hp2 | a0001 | c0004 | t0002 | g0032 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0250 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0207 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0144 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02818 | hp2 | a0005 | c0010 | t0002 | g0143 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0168 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02895 | hp2 | a0001 | c0006 | t0001 | g0171 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02965 | hp1 | a0001 | c0012 | t0001 | g0145 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0067 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02976 | hp1 | a0001 | c0004 | t0003 | g0027 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0167 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03041 | hp2 | a0001 | c0006 | t0001 | g0172 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03139 | hp1 | a0001 | c0007 | t0002 | g0142 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03209 | hp1 | a0001 | c0004 | t0003 | g0021 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03209 | hp2 | a0001 | c0009 | t0002 | g0329 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03239 | hp1 | a0001 | c0004 | t0011 | g0004 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03239 | hp2 | a0001 | c0004 | t0002 | g0035 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03453 | hp2 | a0001 | c0006 | t0001 | g0174 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0152 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03491 | hp1 | a0001 | c0003 | t0007 | g0164 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03516 | hp1 | a0006 | c0013 | t0001 | g0228 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0081 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0049 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03704 | hp2 | a0001 | c0004 | t0003 | g0022 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03710 | hp2 | a0001 | c0004 | t0003 | g0034 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03831 | hp1 | a0001 | c0003 | t0001 | g0208 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0259 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03927 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0146 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0155 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0166 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0151 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04228 | hp2 | a0001 | c0003 | t0002 | g0047 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0064 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18612 | hp1 | a0001 | c0017 | t0001 | g0263 | EAS | CHB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0169 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18957 | hp2 | a0001 | c0002 | t0008 | g0125 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18962 | hp2 | a0001 | c0016 | t0001 | g0235 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18966 | hp2 | a0001 | c0005 | t0001 | g0116 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18970 | hp2 | a0001 | c0005 | t0001 | g0109 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18971 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18971 | hp2 | a0007 | c0020 | t0001 | g0201 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18977 | hp1 | a0001 | c0005 | t0001 | g0121 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18979 | hp1 | a0008 | c0015 | t0001 | g0332 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18980 | hp2 | a0001 | c0004 | t0003 | g0036 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18985 | hp1 | a0009 | c0019 | t0001 | g0320 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18989 | hp1 | a0010 | c0022 | t0001 | g0134 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18990 | hp2 | a0001 | c0005 | t0001 | g0120 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18991 | hp1 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18994 | hp1 | a0001 | c0003 | t0002 | g0046 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19010 | hp2 | a0001 | c0005 | t0001 | g0118 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19011 | hp1 | a0001 | c0002 | t0013 | g0086 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19030 | hp1 | a0001 | c0004 | t0002 | g0030 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19056 | hp2 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19070 | hp1 | a0001 | c0005 | t0001 | g0115 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19080 | hp2 | a0001 | c0002 | t0012 | g0132 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19087 | hp2 | a0001 | c0004 | t0003 | g0033 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ASW | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ASW | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20752 | hp1 | a0001 | c0004 | t0002 | g0211 | EUR | TSI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0162 | EUR | TSI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | GIH | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | GIH | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0219 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01123 | hp2 | a0001 | c0007 | t0002 | g0328 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0066 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02109 | hp2 | a0003 | c0021 | t0001 | g0138 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02559 | hp2 | a0001 | c0004 | t0002 | g0044 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | USA | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20300 | hp1 | a0001 | c0006 | t0001 | g0173 | AFR | USA | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | USA | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0104 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0304 | REF | REF | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0105 | REF | REF | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17754311 | TTGCAGAT others(13): Show |
T | 1 | a0001 | 1 | NA19011.hp1 | splice_acceptor_variant&splice_region_variant&5_prime_UTR_variant&intron_variant | HIGH | c.-182-5_-168delTGCA others(16): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/29 | 834 | chr19 | 17754311 | ||||||
chr19:17764410 | C | T | 1 | a0005 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.155C>T | p.Ala52Val | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/29 | 438/3208 | 155/2670 | 52/889 | chr19 | 17764410 | |||
chr19:17766690 | G | T | 1 | a0010 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.216G>T | p.Glu72Asp | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/29 | 499/3208 | 216/2670 | 72/889 | chr19 | 17766690 | |||
chr19:17770831 | C | T | 1 | a0003 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.529C>T | p.Arg177Cys | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/29 | 812/3208 | 529/2670 | 177/889 | chr19 | 17770831 | |||
chr19:17774415 | C | T | 1 | a0007 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.857C>T | p.Ala286Val | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/29 | 1140/3208 | 857/2670 | 286/889 | chr19 | 17774415 | |||
chr19:17774444 | C | G | 1 | a0009 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.886C>G | p.Arg296Gly | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/29 | 1169/3208 | 886/2670 | 296/889 | chr19 | 17774444 | |||
chr19:17774447 | C | G | 1 | a0009 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.889C>G | p.Arg297Gly | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/29 | 1172/3208 | 889/2670 | 297/889 | chr19 | 17774447 | |||
chr19:17775486 | A | T | 1 | a0002 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.976A>T | p.Thr326Ser | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/29 | 1259/3208 | 976/2670 | 326/889 | chr19 | 17775486 | |||
chr19:17784795 | C | A | 1 | a0006 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.2297C>A | p.Thr766Asn | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/29 | 2580/3208 | 2297/2670 | 766/889 | chr19 | 17784795 | |||
chr19:17784899 | G | A | 1 | a0004 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2401G>A | p.Val801Ile | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/29 | 2684/3208 | 2401/2670 | 801/889 | chr19 | 17784899 | |||
chr19:17787783 | G | A | 1 | a0008 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.2584G>A | p.Val862Met | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/29 | 2867/3208 | 2584/2670 | 862/889 | chr19 | 17787783 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17755170 | G | A | 1 | a0001c0008 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.6G>A | p.Ser2Ser | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/29 | 289/3208 | 6/2670 | 2/889 | chr19 | 17755170 | |||
chr19:17755179 | G | C | 3 | a0001c0007 a0001c0009 a0005c0010 |
5 | HG01123.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.15G>C | p.Gly5Gly | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/29 | 298/3208 | 15/2670 | 5/889 | chr19 | 17755179 | |||
chr19:17766765 | G | A | 1 | a0001c0011 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.291G>A | p.Lys97Lys | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/29 | 574/3208 | 291/2670 | 97/889 | chr19 | 17766765 | |||
chr19:17774446 | G | C | 1 | a0009c0019 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.888G>C | p.Arg296Arg | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/29 | 1171/3208 | 888/2670 | 296/889 | chr19 | 17774446 | |||
chr19:17774461 | A | G | 13 | a0001c0001 a0001c0005 a0001c0006 others(10): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
synonymous_variant | LOW | c.903A>G | p.Pro301Pro | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/29 | 1186/3208 | 903/2670 | 301/889 | chr19 | 17774461 | |||
chr19:17775071 | C | T | 2 | a0001c0004 a0001c0008 |
35 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(32): Show |
synonymous_variant | LOW | c.936C>T | p.Pro312Pro | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 14/29 | 1219/3208 | 936/2670 | 312/889 | chr19 | 17775071 | |||
chr19:17776131 | G | A | 12 | a0001c0001 a0001c0006 a0001c0009 others(9): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
synonymous_variant | LOW | c.1152G>A | p.Ala384Ala | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 16/29 | 1435/3208 | 1152/2670 | 384/889 | chr19 | 17776131 | |||
chr19:17781283 | A | G | 1 | a0001c0017 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.1680A>G | p.Pro560Pro | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 21/29 | 1963/3208 | 1680/2670 | 560/889 | chr19 | 17781283 | |||
chr19:17781782 | A | G | 16 | a0001c0001 a0001c0003 a0001c0004 others(13): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
synonymous_variant | LOW | c.1899A>G | p.Thr633Thr | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/29 | 2182/3208 | 1899/2670 | 633/889 | chr19 | 17781782 | |||
chr19:17781794 | C | T | 2 | a0001c0012 a0001c0016 |
2 | HG02965.hp1 NA18962.hp2 |
synonymous_variant | LOW | c.1911C>T | p.His637His | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/29 | 2194/3208 | 1911/2670 | 637/889 | chr19 | 17781794 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17751531 | G | A | 1 | a0001c0002t0008 | 1 | NA18957.hp2 | 5_prime_UTR_variant | MODIFIER | c.-229G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/29 | 3634 | chr19 | 17751531 | ||||||
chr19:17754340 | T | G | 1 | a0001c0001t0009 | 1 | HG02523.hp1 | 5_prime_UTR_variant | MODIFIER | c.-159T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/29 | 825 | chr19 | 17754340 | ||||||
chr19:17754341 | G | A | 1 | a0001c0004t0010 | 1 | HG01993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-158G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/29 | 824 | chr19 | 17754341 | ||||||
chr19:17754667 | A | G | 2 | a0001c0003t0004 a0001c0003t0007 |
6 | HG01099.hp2 HG01175.hp2 HG01516.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-62A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/29 | chr19 | 17754667 | |||||||
chr19:17754670 | T | G | 13 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 others(10): Show |
47 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-59T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/29 | 495 | chr19 | 17754670 | ||||||
chr19:17755155 | G | A | 1 | a0001c0002t0012 | 1 | NA19080.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/29 | 10 | chr19 | 17755155 | ||||||
chr19:17788324 | C | T | 1 | a0001c0002t0006 | 2 | HG02055.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*18C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 29/29 | 18 | chr19 | 17788324 | ||||||
chr19:17788457 | C | G | 1 | a0001c0004t0011 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*151C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 29/29 | 151 | chr19 | 17788457 | ||||||
chr19:17788458 | C | T | 5 | a0001c0001t0005 a0001c0003t0007 a0001c0004t0003 others(2): Show |
15 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*152C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 29/29 | 152 | chr19 | 17788458 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17751608 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-183+31A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17751608 | |||||||
chr19:17751727 | C | T | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-183+150C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17751727 | |||||||
chr19:17751819 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-183+242C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17751819 | |||||||
chr19:17752116 | C | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(158): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.-183+539C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752116 | |||||||
chr19:17752149 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-183+572A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752149 | |||||||
chr19:17752158 | C | T | 1 | a0001c0002t0001g0179 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-183+581C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752158 | |||||||
chr19:17752226 | T | TTGTA | 16 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 others(13): Show |
16 | HG01167.hp1 HG01169.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.-183+679_-183+682d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752226 | ||||||
chr19:17752226 | T | TTGTATGT others(1): Show |
40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(37): Show |
41 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-183+675_-183+682d others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752226 | ||||||
chr19:17752226 | TTGTA | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(190): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-183+679_-183+682d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752226 | ||||||
chr19:17752226 | TTGTATGT others(5): Show |
T | 2 | a0001c0001t0001g0333 a0001c0001t0001g0335 |
2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-183+671_-183+682d others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752226 | ||||||
chr19:17752304 | G | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(250): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.-183+727G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752304 | |||||||
chr19:17752345 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-183+768G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752345 | |||||||
chr19:17752345 | G | T | 2 | a0001c0002t0002g0064 a0001c0011t0002g0063 |
2 | HG01358.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-183+768G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752345 | |||||||
chr19:17752361 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-183+784T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752361 | |||||||
chr19:17752416 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-183+839G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752416 | |||||||
chr19:17752485 | C | T | 4 | a0001c0002t0001g0137 a0001c0002t0001g0139 a0001c0002t0001g0140 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-183+908C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752485 | |||||||
chr19:17752508 | CCTCGGCC others(17): Show |
C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-183+932_-183+955d others(26): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752508 | |||||||
chr19:17752512 | G | A | 110 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(107): Show |
113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-183+935G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752512 | |||||||
chr19:17752534 | A | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-183+957A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752534 | |||||||
chr19:17752535 | C | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-183+958C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752535 | |||||||
chr19:17752736 | C | CA | 170 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(167): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-183+1176dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752736 | ||||||
chr19:17752736 | C | CAA | 9 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(6): Show |
9 | HG01192.hp2 HG02132.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.-183+1175_-183+117 others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752736 | ||||||
chr19:17752754 | T | A | 12 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(9): Show |
12 | HG01167.hp1 HG01169.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-183+1177T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752754 | |||||||
chr19:17752833 | G | A | 2 | a0001c0004t0002g0017 a0001c0004t0002g0018 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-183+1256G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752833 | |||||||
chr19:17752842 | A | G | 2 | a0001c0002t0002g0064 a0001c0011t0002g0063 |
2 | HG01358.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-183+1265A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752842 | |||||||
chr19:17752919 | T | A | 1 | a0007c0020t0001g0201 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-183+1342T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752919 | |||||||
chr19:17753037 | G | A | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-182-1280G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753037 | |||||||
chr19:17753069 | G | A | 10 | a0001c0001t0001g0028 a0001c0001t0002g0024 a0001c0003t0001g0019 others(7): Show |
10 | HG00323.hp2 HG00733.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-182-1248G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753069 | |||||||
chr19:17753184 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-182-1133A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753184 | |||||||
chr19:17753235 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-182-1082G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753235 | |||||||
chr19:17753236 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(249): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.-182-1081T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753236 | |||||||
chr19:17753303 | A | C | 4 | a0001c0002t0002g0049 a0001c0003t0002g0046 a0001c0003t0002g0047 others(1): Show |
4 | HG03688.hp2 HG04228.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.-182-1014A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753303 | |||||||
chr19:17753394 | C | T | 38 | a0001c0001t0001g0028 a0001c0001t0002g0024 a0001c0002t0002g0049 others(35): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.-182-923C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753394 | |||||||
chr19:17753545 | A | G | 248 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(245): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.-182-772A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753545 | |||||||
chr19:17753643 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(249): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.-182-674T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753643 | |||||||
chr19:17753705 | C | T | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | NA18968.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-182-612C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753705 | |||||||
chr19:17753891 | T | C | 251 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(248): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.-182-426T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753891 | |||||||
chr19:17754009 | G | T | 1 | a0001c0001t0001g0338 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-182-308G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17754009 | |||||||
chr19:17754111 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-182-206C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17754111 | |||||||
chr19:17754400 | G | T | 1 | a0001c0005t0001g0136 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-138+39G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/28 | chr19 | 17754400 | |||||||
chr19:17754433 | G | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-138+72G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/28 | chr19 | 17754433 | |||||||
chr19:17754496 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(251): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-137-96T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/28 | chr19 | 17754496 | |||||||
chr19:17754759 | G | T | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0008c0015t0001g0332 |
3 | HG02523.hp2 NA18979.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-48+78G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/28 | chr19 | 17754759 | |||||||
chr19:17754768 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-48+87C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/28 | chr19 | 17754768 | |||||||
chr19:17754964 | G | T | 1 | a0001c0012t0001g0145 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-47-154G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/28 | chr19 | 17754964 | |||||||
chr19:17755032 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-47-86T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/28 | chr19 | 17755032 | |||||||
chr19:17755266 | T | A | 1 | a0004c0014t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.27+75T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17755266 | |||||||
chr19:17755379 | C | A | 1 | a0001c0001t0001g0009 | 2 | HG00733.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.27+188C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17755379 | |||||||
chr19:17755391 | A | G | 1 | a0001c0002t0001g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.27+200A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17755391 | |||||||
chr19:17755538 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(247): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.27+347C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17755538 | |||||||
chr19:17755675 | T | TA | 34 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0151 others(31): Show |
36 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.27+485dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17755675 | ||||||
chr19:17755936 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(234): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.27+745T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17755936 | |||||||
chr19:17756024 | A | G | 2 | a0001c0002t0001g0141 a0001c0012t0001g0145 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.27+833A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756024 | |||||||
chr19:17756144 | T | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.27+953T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756144 | |||||||
chr19:17756244 | C | T | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.27+1053C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756244 | |||||||
chr19:17756370 | G | A | 3 | a0001c0003t0004g0148 a0001c0003t0004g0149 a0001c0003t0007g0150 |
3 | HG01516.hp2 HG01517.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.27+1179G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756370 | |||||||
chr19:17756646 | C | T | 1 | a0001c0002t0002g0049 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27+1455C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756646 | |||||||
chr19:17756733 | G | A | 4 | a0001c0002t0002g0049 a0001c0003t0002g0046 a0001c0003t0002g0047 others(1): Show |
4 | HG03688.hp2 HG04228.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+1542G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756733 | |||||||
chr19:17756737 | T | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.27+1546T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756737 | |||||||
chr19:17756765 | C | G | 1 | a0001c0001t0001g0319 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.27+1574C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756765 | |||||||
chr19:17756796 | A | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.27+1605A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756796 | |||||||
chr19:17756803 | T | C | 31 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0151 others(28): Show |
33 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.27+1612T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756803 | |||||||
chr19:17756821 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.27+1630G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756821 | |||||||
chr19:17756915 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
7 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+1724G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756915 | |||||||
chr19:17757087 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.27+1896G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757087 | |||||||
chr19:17757114 | G | A | 89 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 others(86): Show |
92 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.27+1923G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757114 | |||||||
chr19:17757165 | T | C | 1 | a0001c0002t0001g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.27+1974T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757165 | |||||||
chr19:17757170 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.27+1979T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757170 | |||||||
chr19:17757177 | C | A | 2 | a0001c0003t0004g0148 a0001c0003t0004g0149 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.27+1986C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757177 | |||||||
chr19:17757182 | T | TA | 32 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0053 others(29): Show |
32 | HG00639.hp1 HG00735.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.27+2013dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17757182 | ||||||
chr19:17757182 | TA | T | 9 | a0001c0001t0001g0318 a0001c0004t0002g0045 a0001c0005t0001g0135 others(6): Show |
9 | HG01070.hp1 HG01943.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+2013delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17757182 | ||||||
chr19:17757303 | A | G | 50 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.27+2112A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757303 | |||||||
chr19:17757401 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.27+2210G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757401 | |||||||
chr19:17757401 | G | C | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2210G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757401 | |||||||
chr19:17757405 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | NA18968.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.27+2214G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757405 | |||||||
chr19:17757457 | C | T | 2 | a0001c0002t0001g0141 a0001c0012t0001g0145 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.27+2266C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757457 | |||||||
chr19:17757477 | G | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2286G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757477 | |||||||
chr19:17757485 | G | C | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2294G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757485 | |||||||
chr19:17757505 | T | A | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2314T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757505 | |||||||
chr19:17757512 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27+2321A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757512 | |||||||
chr19:17757520 | G | A | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2329G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757520 | |||||||
chr19:17757550 | A | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2359A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757550 | |||||||
chr19:17757557 | A | AAGGTGGA others(4): Show |
1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2366_27+2367ins others(11): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757557 | |||||||
chr19:17757558 | G | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2367G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757558 | |||||||
chr19:17757562 | C | A | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2371C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757562 | |||||||
chr19:17757564 | C | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2373C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757564 | |||||||
chr19:17757567 | T | A | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2376T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757567 | |||||||
chr19:17757569 | C | A | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2378C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757569 | |||||||
chr19:17757570 | G | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2379G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757570 | |||||||
chr19:17757579 | G | A | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2388G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757579 | |||||||
chr19:17757602 | A | G | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2411A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757602 | |||||||
chr19:17757610 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.27+2419C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757610 | |||||||
chr19:17757612 | A | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2421A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757612 | |||||||
chr19:17757633 | A | G | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2442A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757633 | |||||||
chr19:17757634 | G | A | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2443G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757634 | |||||||
chr19:17757653 | C | T | 3 | a0001c0003t0001g0167 a0001c0003t0001g0168 a0001c0003t0001g0169 |
3 | HG02886.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.27+2462C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757653 | |||||||
chr19:17757658 | G | C | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2467G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757658 | |||||||
chr19:17757660 | A | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2469A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757660 | |||||||
chr19:17757663 | C | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2472C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757663 | |||||||
chr19:17757664 | C | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2473C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757664 | |||||||
chr19:17757665 | A | C | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2474A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757665 | |||||||
chr19:17757666 | A | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2475A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757666 | |||||||
chr19:17757667 | A | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2476A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757667 | |||||||
chr19:17757674 | G | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2483G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757674 | |||||||
chr19:17757675 | A | C | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2484A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757675 | |||||||
chr19:17757676 | G | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2485G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757676 | |||||||
chr19:17757677 | A | C | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2486A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757677 | |||||||
chr19:17757678 | A | C | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2487A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757678 | |||||||
chr19:17757679 | G | C | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2488G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757679 | |||||||
chr19:17757682 | G | A | 5 | a0001c0006t0001g0171 a0001c0006t0001g0172 a0001c0006t0001g0173 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+2491G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757682 | |||||||
chr19:17757682 | G | C | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2491G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757682 | |||||||
chr19:17757683 | A | T | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2492A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757683 | |||||||
chr19:17757694 | C | T | 5 | a0001c0001t0001g0170 a0001c0002t0002g0064 a0001c0002t0002g0066 others(2): Show |
5 | HG01358.hp1 HG02109.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+2503C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757694 | |||||||
chr19:17757894 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.27+2703C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757894 | |||||||
chr19:17757915 | C | A | 1 | a0001c0002t0013g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2724C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757915 | |||||||
chr19:17757915 | C | CA | 30 | a0001c0001t0001g0053 a0001c0001t0001g0087 a0001c0001t0001g0181 others(27): Show |
30 | HG01123.hp1 HG01261.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.27+2744dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17757915 | ||||||
chr19:17757915 | CA | C | 9 | a0001c0001t0001g0183 a0001c0001t0001g0202 a0001c0001t0001g0203 others(6): Show |
9 | HG01243.hp1 HG01516.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+2744delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17757915 | ||||||
chr19:17757915 | CAA | C | 32 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0141 others(29): Show |
34 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.27+2743_27+2744del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17757915 | ||||||
chr19:17757982 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.27+2791G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757982 | |||||||
chr19:17758102 | C | T | 5 | a0001c0006t0001g0171 a0001c0006t0001g0172 a0001c0006t0001g0173 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+2911C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758102 | |||||||
chr19:17758132 | G | A | 1 | a0001c0012t0001g0145 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.27+2941G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758132 | |||||||
chr19:17758572 | T | C | 1 | a0006c0013t0001g0228 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.27+3381T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758572 | |||||||
chr19:17758789 | A | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0080 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.27+3598A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758789 | |||||||
chr19:17758825 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
7 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+3634C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758825 | |||||||
chr19:17758835 | C | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(293): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.27+3644C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758835 | |||||||
chr19:17758925 | G | T | 2 | a0001c0002t0002g0066 a0001c0002t0002g0067 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.27+3734G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758925 | |||||||
chr19:17758992 | A | G | 2 | a0001c0001t0001g0313 a0001c0001t0001g0314 |
2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.28-3770A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758992 | |||||||
chr19:17759009 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(293): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.28-3753G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759009 | |||||||
chr19:17759036 | G | T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(166): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.28-3726G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759036 | |||||||
chr19:17759084 | G | A | 3 | a0001c0001t0001g0229 a0001c0001t0001g0324 a0001c0001t0001g0325 |
3 | HG03834.hp2 NA18968.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.28-3678G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759084 | |||||||
chr19:17759101 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.28-3661T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759101 | |||||||
chr19:17759136 | A | T | 3 | a0001c0002t0002g0064 a0001c0003t0001g0104 a0001c0011t0002g0063 |
3 | HG01358.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-3626A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759136 | |||||||
chr19:17759200 | A | G | 1 | a0001c0004t0002g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.28-3562A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759200 | |||||||
chr19:17759226 | C | CT | 119 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(116): Show |
124 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.28-3522dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | ||||||
chr19:17759226 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0217 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG03490.hp1 NA18965.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.28-3533_28-3522dup others(12): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | ||||||
chr19:17759226 | C | CTTTTTTT others(6): Show |
145 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.28-3534_28-3522dup others(13): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | ||||||
chr19:17759226 | C | CTTTTTTT others(7): Show |
62 | a0001c0001t0001g0006 a0001c0001t0001g0065 a0001c0001t0001g0073 others(59): Show |
63 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.28-3535_28-3522dup others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | ||||||
chr19:17759226 | C | CTTTTTTT others(8): Show |
4 | a0001c0001t0001g0170 a0001c0001t0001g0215 a0001c0003t0001g0312 others(1): Show |
4 | HG00741.hp1 HG01358.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-3522_28-3521ins others(15): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | ||||||
chr19:17759226 | C | CTTTTTTT others(9): Show |
1 | a0001c0003t0001g0144 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.28-3522_28-3521ins others(16): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | ||||||
chr19:17759655 | G | A | 43 | a0001c0001t0001g0183 a0001c0001t0002g0024 a0001c0002t0001g0141 others(40): Show |
44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.28-3107G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759655 | |||||||
chr19:17759752 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-3010G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759752 | |||||||
chr19:17759812 | TA | T | 43 | a0001c0001t0001g0183 a0001c0001t0002g0024 a0001c0002t0001g0141 others(40): Show |
44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.28-2940delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759812 | ||||||
chr19:17759908 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.28-2854A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759908 | |||||||
chr19:17760009 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28-2753C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760009 | |||||||
chr19:17760047 | CT | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0051 others(73): Show |
79 | HG00423.hp2 HG00639.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.28-2700delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17760047 | ||||||
chr19:17760047 | CTT | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(246): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.28-2701_28-2700del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17760047 | ||||||
chr19:17760115 | G | T | 24 | a0001c0001t0001g0065 a0001c0001t0001g0199 a0001c0001t0001g0200 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.28-2647G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760115 | |||||||
chr19:17760302 | C | T | 2 | a0001c0003t0001g0008 a0001c0003t0001g0153 |
3 | HG01070.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.28-2460C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760302 | |||||||
chr19:17760332 | T | G | 1 | a0001c0006t0001g0171 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.28-2430T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760332 | |||||||
chr19:17760423 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(166): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.28-2339G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760423 | |||||||
chr19:17760547 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.28-2215A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760547 | |||||||
chr19:17760928 | G | C | 217 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.28-1834G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760928 | |||||||
chr19:17760940 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.28-1822C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760940 | |||||||
chr19:17761036 | C | A | 1 | a0001c0002t0001g0205 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.28-1726C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761036 | |||||||
chr19:17761163 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.28-1599C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761163 | |||||||
chr19:17761260 | C | T | 48 | a0001c0001t0001g0183 a0001c0001t0002g0024 a0001c0002t0001g0141 others(45): Show |
49 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.28-1502C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761260 | |||||||
chr19:17761283 | C | T | 48 | a0001c0001t0001g0183 a0001c0001t0002g0024 a0001c0002t0001g0141 others(45): Show |
49 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.28-1479C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761283 | |||||||
chr19:17761401 | C | CT | 247 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(244): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.28-1349dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761401 | ||||||
chr19:17761438 | T | G | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.28-1324T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761438 | |||||||
chr19:17761560 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.28-1202G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761560 | |||||||
chr19:17761633 | C | CAT | 6 | a0001c0002t0001g0151 a0001c0002t0001g0177 a0001c0003t0001g0152 others(3): Show |
6 | HG01496.hp1 HG01516.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-1109_28-1108dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761633 | C | CATAT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.28-1111_28-1108dup others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761633 | C | CATATAT | 28 | a0001c0001t0001g0084 a0001c0001t0001g0184 a0001c0001t0001g0186 others(25): Show |
28 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.28-1113_28-1108dup others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761633 | C | CATATATA others(1): Show |
7 | a0001c0001t0001g0192 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
7 | HG01891.hp2 HG02922.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-1115_28-1108dup others(8): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761633 | C | CATATATA others(3): Show |
12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG02056.hp1 HG02071.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-1117_28-1108dup others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761633 | C | CATATATA others(5): Show |
1 | a0001c0001t0005g0198 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.28-1119_28-1108dup others(12): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761633 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.28-1121_28-1108dup others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761633 | C | CATATATA others(9): Show |
1 | a0001c0001t0001g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.28-1123_28-1108dup others(16): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761633 | C | CATATATA others(11): Show |
1 | a0001c0001t0001g0279 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.28-1125_28-1108dup others(18): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761633 | C | CATATATA others(15): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01175.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.28-1108_28-1107ins others(22): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761633 | CAT | C | 44 | a0001c0001t0001g0170 a0001c0001t0001g0183 a0001c0001t0002g0024 others(41): Show |
45 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.28-1109_28-1108del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | ||||||
chr19:17761653 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0183 |
3 | HG02572.hp2 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.28-1109T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761653 | |||||||
chr19:17761653 | T | TATATATA others(15): Show |
1 | a0001c0001t0001g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.28-1108_28-1107ins others(22): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761653 | ||||||
chr19:17761664 | T | G | 1 | a0001c0001t0001g0335 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.28-1098T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761664 | |||||||
chr19:17761673 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.28-1089G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761673 | |||||||
chr19:17761729 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.28-1033C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761729 | |||||||
chr19:17761905 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.28-857C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761905 | |||||||
chr19:17761927 | A | T | 1 | a0010c0022t0001g0134 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.28-835A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761927 | |||||||
chr19:17761969 | T | TTTCA | 158 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(155): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.28-766_28-763dupCA others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761969 | ||||||
chr19:17761969 | T | TTTCATTC others(1): Show |
54 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0074 others(51): Show |
56 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.28-770_28-763dupCA others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761969 | ||||||
chr19:17761969 | T | TTTCATTC others(5): Show |
4 | a0001c0001t0001g0183 a0001c0004t0002g0031 a0001c0007t0002g0142 others(1): Show |
4 | HG02004.hp2 HG02145.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-774_28-763dupCA others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761969 | ||||||
chr19:17761969 | T | TTTCATTC others(9): Show |
1 | a0001c0001t0001g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28-778_28-763dupCA others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761969 | ||||||
chr19:17762000 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
7 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-762T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762000 | |||||||
chr19:17762027 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.28-735C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762027 | |||||||
chr19:17762214 | G | C | 2 | a0001c0002t0002g0064 a0001c0011t0002g0063 |
2 | HG01358.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.28-548G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762214 | |||||||
chr19:17762287 | A | C | 2 | a0001c0002t0002g0066 a0001c0002t0002g0067 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.28-475A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762287 | |||||||
chr19:17762293 | C | CT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0183 others(18): Show |
22 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.28-455dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17762293 | ||||||
chr19:17762293 | C | CTT | 143 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.28-456_28-455dupTT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17762293 | ||||||
chr19:17762312 | A | G | 5 | a0001c0006t0001g0171 a0001c0006t0001g0172 a0001c0006t0001g0173 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-450A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762312 | |||||||
chr19:17762530 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.28-232C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762530 | |||||||
chr19:17762606 | A | G | 3 | a0001c0004t0001g0178 a0001c0004t0002g0017 a0001c0004t0002g0018 |
3 | HG01257.hp2 HG01258.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.28-156A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762606 | |||||||
chr19:17762923 | A | G | 1 | a0001c0001t0001g0318 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.119+70A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17762923 | |||||||
chr19:17763094 | A | C | 336 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(333): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.119+241A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763094 | |||||||
chr19:17763196 | A | C | 1 | a0001c0003t0001g0270 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.119+343A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763196 | |||||||
chr19:17763259 | C | CT | 8 | a0001c0001t0001g0184 a0001c0001t0001g0307 a0001c0002t0001g0081 others(5): Show |
8 | HG01361.hp1 HG01978.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.119+428dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763259 | ||||||
chr19:17763259 | CT | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(196): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.119+428delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763259 | ||||||
chr19:17763259 | CTT | C | 7 | a0001c0001t0001g0237 a0001c0001t0001g0275 a0001c0001t0001g0290 others(4): Show |
7 | HG00558.hp2 HG02523.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.119+427_119+428del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763259 | ||||||
chr19:17763501 | C | T | 6 | a0001c0002t0001g0092 a0001c0002t0001g0122 a0001c0002t0001g0123 others(3): Show |
6 | NA18945.hp2 NA18957.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.119+648C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763501 | |||||||
chr19:17763530 | G | T | 1 | a0001c0003t0001g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.119+677G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763530 | |||||||
chr19:17763553 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.119+700T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763553 | |||||||
chr19:17763563 | C | CT | 115 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(112): Show |
122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.119+725dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763563 | ||||||
chr19:17763563 | C | CTT | 51 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0080 others(48): Show |
51 | HG00099.hp1 HG00544.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.119+724_119+725dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763563 | ||||||
chr19:17763563 | C | CTTT | 12 | a0001c0001t0001g0195 a0001c0001t0001g0224 a0001c0001t0001g0265 others(9): Show |
12 | HG00280.hp1 HG00423.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.119+723_119+725dup others(3): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763563 | ||||||
chr19:17763563 | CT | C | 29 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0151 others(26): Show |
31 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.119+725delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763563 | ||||||
chr19:17763579 | C | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(217): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.119+726C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763579 | |||||||
chr19:17763650 | C | T | 26 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0151 others(23): Show |
28 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.120-725C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763650 | |||||||
chr19:17763660 | C | T | 3 | a0001c0001t0001g0170 a0001c0002t0002g0064 a0001c0011t0002g0063 |
3 | HG01358.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.120-715C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763660 | |||||||
chr19:17763735 | A | T | 9 | a0001c0001t0001g0193 a0001c0001t0001g0321 a0001c0002t0002g0064 others(6): Show |
9 | HG01358.hp1 HG01993.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.120-640A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763735 | |||||||
chr19:17763789 | C | G | 5 | a0001c0001t0001g0200 a0001c0001t0001g0226 a0001c0001t0001g0308 others(2): Show |
5 | HG00558.hp1 HG02056.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.120-586C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763789 | |||||||
chr19:17763927 | C | T | 1 | a0001c0002t0001g0253 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.120-448C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763927 | |||||||
chr19:17764044 | C | CT | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(162): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.120-318dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17764044 | ||||||
chr19:17764044 | C | CTT | 6 | a0001c0001t0001g0073 a0001c0001t0001g0217 a0001c0001t0001g0278 others(3): Show |
6 | HG02071.hp2 HG02083.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.120-319_120-318dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17764044 | ||||||
chr19:17764165 | C | T | 2 | a0001c0002t0002g0064 a0001c0011t0002g0063 |
2 | HG01358.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.120-210C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17764165 | |||||||
chr19:17764214 | T | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(167): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.120-161T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17764214 | |||||||
chr19:17764336 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0285 |
2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.120-39C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17764336 | |||||||
chr19:17764350 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0233 |
2 | NA18941.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.120-25A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17764350 | |||||||
chr19:17764457 | G | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0194 |
2 | HG01109.hp1 HG01891.hp2 |
splice_region_variant&intron_variant | LOW | c.194+8G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764457 | |||||||
chr19:17764465 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.194+16G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764465 | |||||||
chr19:17764508 | T | A | 1 | a0001c0001t0001g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.194+59T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764508 | |||||||
chr19:17764661 | AGC | A | 43 | a0001c0001t0001g0183 a0001c0001t0002g0024 a0001c0002t0001g0141 others(40): Show |
44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.194+213_194+214del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764661 | |||||||
chr19:17764755 | T | A | 2 | a0001c0002t0002g0066 a0001c0002t0002g0067 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.194+306T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764755 | |||||||
chr19:17764814 | C | G | 6 | a0001c0004t0002g0004 a0001c0004t0002g0015 a0001c0004t0002g0029 others(3): Show |
6 | HG00280.hp2 HG01433.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+365C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764814 | |||||||
chr19:17764815 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.194+366C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764815 | |||||||
chr19:17764871 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.194+422G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764871 | |||||||
chr19:17764896 | C | G | 2 | a0001c0002t0002g0066 a0001c0002t0002g0067 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.194+447C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764896 | |||||||
chr19:17764933 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.194+484G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764933 | |||||||
chr19:17764946 | C | A | 170 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(167): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.194+497C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764946 | |||||||
chr19:17765066 | GA | G | 7 | a0001c0001t0001g0229 a0001c0001t0001g0309 a0001c0001t0001g0315 others(4): Show |
7 | HG02523.hp1 HG03834.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.194+635delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765066 | ||||||
chr19:17765213 | G | A | 3 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0004c0014t0001g0052 |
3 | HG02145.hp2 HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.194+764G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765213 | |||||||
chr19:17765235 | G | GAAGGCCC others(8): Show |
1 | a0001c0001t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.194+787_194+801dup others(15): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765235 | ||||||
chr19:17765255 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.194+806C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765255 | |||||||
chr19:17765306 | G | T | 1 | a0001c0003t0001g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194+857G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765306 | |||||||
chr19:17765384 | C | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.194+935C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765384 | |||||||
chr19:17765530 | G | A | 1 | a0001c0002t0001g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.194+1081G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765530 | |||||||
chr19:17765533 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.194+1084C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765533 | |||||||
chr19:17765682 | C | A | 1 | a0001c0001t0001g0291 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.195-987C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765682 | |||||||
chr19:17765756 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.195-913A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765756 | |||||||
chr19:17765856 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0308 |
2 | HG02056.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.195-813T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765856 | |||||||
chr19:17765882 | C | CT | 35 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0050 others(32): Show |
37 | HG01123.hp2 HG01175.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.195-763dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765882 | ||||||
chr19:17765882 | C | CTT | 27 | a0001c0001t0001g0014 a0001c0001t0002g0024 a0001c0002t0001g0141 others(24): Show |
28 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.195-764_195-763dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765882 | ||||||
chr19:17765882 | C | CTTT | 10 | a0001c0004t0002g0015 a0001c0004t0002g0026 a0001c0004t0002g0030 others(7): Show |
10 | HG00140.hp1 HG01255.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.195-765_195-763dup others(3): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765882 | ||||||
chr19:17765882 | CT | C | 35 | a0001c0001t0001g0073 a0001c0001t0001g0170 a0001c0001t0001g0181 others(32): Show |
35 | HG00280.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.195-763delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765882 | ||||||
chr19:17765882 | CTT | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(127): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.195-764_195-763del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765882 | ||||||
chr19:17765950 | G | T | 16 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(13): Show |
16 | HG00544.hp2 HG01192.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.195-719G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765950 | |||||||
chr19:17766090 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0119 |
2 | HG02135.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.195-579A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17766090 | |||||||
chr19:17766177 | A | AT | 17 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0073 others(14): Show |
17 | HG01175.hp1 HG01175.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.195-475dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17766177 | ||||||
chr19:17766177 | AT | A | 6 | a0001c0001t0001g0275 a0001c0002t0002g0064 a0001c0004t0002g0016 others(3): Show |
6 | HG01358.hp1 NA18522.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-475delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17766177 | ||||||
chr19:17766245 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0334 |
2 | HG00423.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.195-424C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17766245 | |||||||
chr19:17766270 | G | A | 2 | a0001c0002t0002g0066 a0001c0002t0002g0067 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.195-399G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17766270 | |||||||
chr19:17766348 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.195-321G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17766348 | |||||||
chr19:17766414 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.195-255C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17766414 | |||||||
chr19:17766922 | TCCGTTAA others(3): Show |
T | 1 | a0010c0022t0001g0134 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.336+114_336+123del others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17766922 | ||||||
chr19:17767074 | G | GT | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.336+276dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767074 | ||||||
chr19:17767197 | C | A | 41 | a0001c0001t0001g0183 a0001c0003t0001g0144 a0001c0004t0001g0178 others(38): Show |
42 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.336+387C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767197 | |||||||
chr19:17767205 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.336+395A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767205 | |||||||
chr19:17767224 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0268 |
3 | HG00735.hp1 HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.336+414G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767224 | |||||||
chr19:17767333 | A | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
83 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.336+523A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767333 | |||||||
chr19:17767385 | C | T | 12 | a0001c0002t0013g0086 a0001c0005t0001g0001 a0001c0005t0001g0108 others(9): Show |
14 | HG00639.hp2 HG01069.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.336+575C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767385 | |||||||
chr19:17767395 | C | CAAAAAA | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.336+593_336+598dup others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767395 | ||||||
chr19:17767395 | C | CAAAAAAA | 23 | a0001c0001t0001g0051 a0001c0001t0001g0069 a0001c0001t0001g0075 others(20): Show |
23 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.336+592_336+598dup others(7): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767395 | ||||||
chr19:17767395 | CA | C | 82 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 others(79): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.336+598delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767395 | ||||||
chr19:17767431 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.336+621A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767431 | |||||||
chr19:17767557 | A | ACT | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+748_336+749dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767557 | ||||||
chr19:17767563 | T | TA | 75 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0183 others(72): Show |
78 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.336+773dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767563 | ||||||
chr19:17767563 | T | TAA | 8 | a0001c0002t0002g0049 a0001c0003t0001g0155 a0001c0003t0001g0166 others(5): Show |
8 | HG01175.hp2 HG03688.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.336+772_336+773dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767563 | ||||||
chr19:17767563 | T | TC | 13 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(10): Show |
13 | HG00099.hp1 HG02132.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+753_336+754ins others(1): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767563 | |||||||
chr19:17767563 | T | TCA | 139 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(136): Show |
146 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.336+753_336+754ins others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767563 | |||||||
chr19:17767563 | T | TCAA | 26 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0051 others(23): Show |
27 | HG01358.hp2 HG01891.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.336+753_336+754ins others(3): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767563 | |||||||
chr19:17767563 | T | TCAAA | 5 | a0001c0001t0001g0069 a0001c0001t0001g0170 a0001c0002t0002g0064 others(2): Show |
5 | HG01358.hp1 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+753_336+754ins others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767563 | |||||||
chr19:17767563 | TA | T | 8 | a0001c0002t0001g0083 a0001c0002t0001g0089 a0001c0002t0001g0101 others(5): Show |
8 | HG01069.hp2 HG02451.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.336+773delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767563 | ||||||
chr19:17767574 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.336+764A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767574 | |||||||
chr19:17767744 | T | G | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.336+934T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767744 | |||||||
chr19:17767755 | TG | T | 41 | a0001c0001t0001g0183 a0001c0003t0001g0144 a0001c0004t0001g0178 others(38): Show |
42 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.336+946delG | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767755 | |||||||
chr19:17767870 | T | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1060T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767870 | |||||||
chr19:17767913 | A | G | 128 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(125): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.336+1103A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767913 | |||||||
chr19:17767966 | T | C | 2 | a0001c0002t0002g0066 a0001c0002t0002g0067 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.336+1156T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767966 | |||||||
chr19:17768024 | T | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1214T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768024 | |||||||
chr19:17768042 | G | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1232G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768042 | |||||||
chr19:17768082 | T | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1272T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768082 | |||||||
chr19:17768126 | G | A | 34 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0151 others(31): Show |
36 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.336+1316G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768126 | |||||||
chr19:17768157 | C | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1347C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768157 | |||||||
chr19:17768213 | T | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1403T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768213 | |||||||
chr19:17768295 | C | T | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1485C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768295 | |||||||
chr19:17768324 | C | A | 1 | a0001c0003t0001g0312 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.336+1514C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768324 | |||||||
chr19:17768386 | T | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.336+1576T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768386 | |||||||
chr19:17768411 | G | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.336+1601G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768411 | |||||||
chr19:17768553 | G | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0051 others(16): Show |
20 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.336+1743G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768553 | |||||||
chr19:17768584 | C | T | 34 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0151 others(31): Show |
36 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.336+1774C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768584 | |||||||
chr19:17768589 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.336+1779G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768589 | |||||||
chr19:17768590 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.336+1780A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768590 | |||||||
chr19:17768618 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(265): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.337-1807T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768618 | |||||||
chr19:17768618 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.337-1807T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768618 | |||||||
chr19:17768638 | C | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1787C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768638 | |||||||
chr19:17768649 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.337-1776G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768649 | |||||||
chr19:17768709 | C | CA | 56 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(53): Show |
59 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.337-1702dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17768709 | ||||||
chr19:17768723 | A | AAG | 6 | a0001c0001t0001g0193 a0001c0001t0001g0223 a0001c0001t0001g0241 others(3): Show |
6 | HG02027.hp1 HG02083.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-1702_337-1701i others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768723 | |||||||
chr19:17768724 | G | A | 31 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(28): Show |
32 | HG01175.hp1 HG01358.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.337-1701G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768724 | |||||||
chr19:17768724 | G | GA | 155 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(152): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.337-1701_337-1700i others(3): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768724 | |||||||
chr19:17768745 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(22): Show |
26 | HG01175.hp1 HG01358.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.337-1680C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768745 | |||||||
chr19:17768760 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01175.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.337-1665T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768760 | |||||||
chr19:17768782 | G | A | 5 | a0001c0006t0001g0171 a0001c0006t0001g0172 a0001c0006t0001g0173 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-1643G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768782 | |||||||
chr19:17768823 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1602C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768823 | |||||||
chr19:17768984 | T | TA | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.337-1431dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17768984 | ||||||
chr19:17769049 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.337-1376G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769049 | |||||||
chr19:17769086 | G | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1339G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769086 | |||||||
chr19:17769148 | G | C | 34 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0151 others(31): Show |
36 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.337-1277G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769148 | |||||||
chr19:17769227 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1198A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769227 | |||||||
chr19:17769241 | C | T | 3 | a0001c0003t0001g0167 a0001c0003t0001g0168 a0001c0003t0001g0169 |
3 | HG02886.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-1184C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769241 | |||||||
chr19:17769274 | C | CA | 48 | a0001c0001t0001g0107 a0001c0001t0001g0154 a0001c0001t0001g0156 others(45): Show |
50 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.337-1131dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769274 | ||||||
chr19:17769274 | C | CAAAA | 135 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.337-1134_337-1131d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769274 | ||||||
chr19:17769274 | C | CAAAAA | 42 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0051 others(39): Show |
42 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.337-1135_337-1131d others(7): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769274 | ||||||
chr19:17769274 | CA | C | 34 | a0001c0001t0001g0183 a0001c0004t0002g0003 a0001c0004t0002g0004 others(31): Show |
35 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.337-1131delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769274 | ||||||
chr19:17769358 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0196 others(14): Show |
20 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.337-1067C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769358 | |||||||
chr19:17769425 | G | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1000G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769425 | |||||||
chr19:17769443 | G | A | 1 | a0001c0002t0001g0106 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.337-982G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769443 | |||||||
chr19:17769449 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.337-976G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769449 | |||||||
chr19:17769462 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.337-963T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769462 | |||||||
chr19:17769495 | C | T | 34 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0151 others(31): Show |
36 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.337-930C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769495 | |||||||
chr19:17769535 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.337-890C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769535 | |||||||
chr19:17769572 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.337-853T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769572 | |||||||
chr19:17769579 | AAACACAC others(10): Show |
A | 1 | a0001c0003t0001g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.337-844_337-828del others(17): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769579 | ||||||
chr19:17769580 | AAC | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0229 a0001c0001t0001g0241 others(16): Show |
19 | HG00609.hp2 HG00673.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.337-793_337-792del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769580 | AACAC | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(64): Show |
69 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.337-795_337-792del others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769580 | AACACAC | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(80): Show |
86 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.337-797_337-792del others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769580 | AACACACA others(1): Show |
A | 26 | a0001c0001t0001g0056 a0001c0001t0001g0074 a0001c0001t0001g0075 others(23): Show |
26 | HG01256.hp2 HG01261.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.337-799_337-792del others(8): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769580 | AACACACA others(3): Show |
A | 35 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0054 others(32): Show |
36 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.337-801_337-792del others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769580 | AACACACA others(5): Show |
A | 32 | a0001c0001t0001g0183 a0001c0001t0001g0192 a0001c0001t0001g0214 others(29): Show |
32 | HG00140.hp1 HG01255.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.337-803_337-792del others(12): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769580 | AACACACA others(7): Show |
A | 14 | a0001c0001t0001g0170 a0001c0002t0001g0088 a0001c0003t0001g0019 others(11): Show |
14 | HG00323.hp2 HG00733.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.337-805_337-792del others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769580 | AACACACA others(9): Show |
A | 32 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0154 others(29): Show |
35 | HG00323.hp1 HG01070.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.337-807_337-792del others(16): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769580 | AACACACA others(11): Show |
A | 8 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0002t0001g0151 others(5): Show |
8 | HG00140.hp2 HG00741.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-809_337-792del others(18): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769580 | AACACACA others(13): Show |
A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0069 others(7): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.337-811_337-792del others(20): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769580 | AACACACA others(17): Show |
A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.337-815_337-792del others(24): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | ||||||
chr19:17769628 | CACACA | C | 3 | a0001c0001t0001g0305 a0001c0002t0006g0185 a0001c0017t0001g0263 |
3 | HG00741.hp2 HG02055.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.337-795_337-791del others(5): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769628 | ||||||
chr19:17769632 | C | A | 1 | a0001c0005t0001g0116 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.337-793C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769632 | |||||||
chr19:17769638 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.337-787G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769638 | |||||||
chr19:17769652 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG00099.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.337-773C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769652 | |||||||
chr19:17769688 | G | C | 5 | a0001c0006t0001g0171 a0001c0006t0001g0172 a0001c0006t0001g0173 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-737G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769688 | |||||||
chr19:17769752 | T | C | 1 | a0001c0001t0001g0330 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.337-673T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769752 | |||||||
chr19:17769819 | T | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-606T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769819 | |||||||
chr19:17769839 | C | CT | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-578dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769839 | ||||||
chr19:17769890 | G | A | 34 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0151 others(31): Show |
36 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.337-535G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769890 | |||||||
chr19:17769909 | A | T | 34 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0151 others(31): Show |
36 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.337-516A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769909 | |||||||
chr19:17769996 | G | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.337-429G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769996 | |||||||
chr19:17770021 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.337-404C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17770021 | |||||||
chr19:17770318 | A | AAC | 3 | a0001c0001t0001g0009 a0001c0002t0002g0066 a0001c0002t0002g0067 |
4 | HG00733.hp1 HG02109.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.337-93_337-92dupCA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17770318 | ||||||
chr19:17770332 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0285 |
2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.337-93C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17770332 | |||||||
chr19:17770362 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.337-63G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17770362 | |||||||
chr19:17770415 | T | C | 5 | a0001c0006t0001g0171 a0001c0006t0001g0172 a0001c0006t0001g0173 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-10T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17770415 | |||||||
chr19:17770421 | G | A | 1 | a0001c0005t0001g0135 | 1 | HG01943.hp2 | splice_region_variant&intron_variant | LOW | c.337-4G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17770421 | |||||||
chr19:17770597 | G | A | 2 | a0001c0001t0001g0335 a0004c0014t0001g0052 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.489+20G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770597 | |||||||
chr19:17770666 | G | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.489+89G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770666 | |||||||
chr19:17770677 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.489+100C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770677 | |||||||
chr19:17770704 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.490-88C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770704 | |||||||
chr19:17770743 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.490-49C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770743 | |||||||
chr19:17770744 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.490-48C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770744 | |||||||
chr19:17771025 | G | A | 39 | a0001c0004t0001g0111 a0001c0004t0001g0178 a0001c0004t0002g0003 others(36): Show |
40 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.594+129G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771025 | |||||||
chr19:17771130 | G | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(17): Show |
21 | HG01175.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.594+234G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771130 | |||||||
chr19:17771219 | T | G | 1 | a0001c0002t0001g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.594+323T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771219 | |||||||
chr19:17771237 | G | A | 6 | a0001c0006t0001g0171 a0001c0006t0001g0172 a0001c0006t0001g0173 others(3): Show |
6 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.594+341G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771237 | |||||||
chr19:17771295 | G | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0053 others(8): Show |
11 | HG02145.hp1 HG02451.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.594+399G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771295 | |||||||
chr19:17771309 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0061 others(2): Show |
5 | HG02145.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+413T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771309 | |||||||
chr19:17771345 | C | A | 1 | a0001c0002t0001g0101 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.594+449C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771345 | |||||||
chr19:17771358 | T | TA | 14 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 others(11): Show |
14 | HG01175.hp1 HG01496.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.594+474dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr19 | 17771358 | ||||||
chr19:17771367 | A | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01243.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.594+471A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771367 | |||||||
chr19:17771370 | AG | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0069 others(46): Show |
51 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.594+475delG | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771370 | |||||||
chr19:17771371 | G | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(217): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.594+475G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771371 | |||||||
chr19:17771387 | G | C | 1 | a0001c0002t0001g0101 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.594+491G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771387 | |||||||
chr19:17771389 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.594+493C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771389 | |||||||
chr19:17771520 | T | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0338 |
2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.594+624T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771520 | |||||||
chr19:17771585 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.594+689C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771585 | |||||||
chr19:17771589 | A | T | 1 | a0001c0001t0005g0198 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.594+693A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771589 | |||||||
chr19:17771605 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.594+709C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771605 | |||||||
chr19:17771626 | G | A | 6 | a0001c0002t0001g0093 a0001c0002t0001g0129 a0001c0002t0001g0130 others(3): Show |
6 | NA18963.hp1 NA18985.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+730G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771626 | |||||||
chr19:17771739 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.595-718A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771739 | |||||||
chr19:17771874 | G | A | 2 | a0001c0003t0001g0168 a0001c0003t0001g0169 |
2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.595-583G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771874 | |||||||
chr19:17772003 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.595-454G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772003 | |||||||
chr19:17772054 | A | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.595-403A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772054 | |||||||
chr19:17772113 | T | C | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.595-344T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772113 | |||||||
chr19:17772174 | T | TTG | 3 | a0001c0001t0001g0229 a0001c0001t0001g0324 a0001c0001t0001g0325 |
3 | HG03834.hp2 NA18968.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.595-266_595-265dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr19 | 17772174 | ||||||
chr19:17772174 | TTG | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(160): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.595-266_595-265del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr19 | 17772174 | ||||||
chr19:17772218 | G | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 others(1): Show |
4 | HG01175.hp1 HG01496.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.595-239G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772218 | |||||||
chr19:17772264 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
22 | HG01175.hp1 HG01496.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.595-193A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772264 | |||||||
chr19:17772266 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.595-191A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772266 | |||||||
chr19:17772425 | C | G | 6 | a0001c0006t0001g0171 a0001c0006t0001g0172 a0001c0006t0001g0173 others(3): Show |
6 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-32C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772425 | |||||||
chr19:17772630 | G | A | 4 | a0001c0002t0002g0049 a0001c0003t0002g0046 a0001c0003t0002g0047 others(1): Show |
4 | HG03688.hp2 HG04228.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-15G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 10/28 | chr19 | 17772630 | |||||||
chr19:17772818 | AT | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0097 others(10): Show |
14 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.790+87delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 17772818 | ||||||
chr19:17772882 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.790+141C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17772882 | |||||||
chr19:17772955 | A | T | 3 | a0001c0001t0001g0258 a0001c0001t0001g0300 a0001c0001t0001g0302 |
3 | HG00280.hp1 HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.790+214A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17772955 | |||||||
chr19:17772964 | GGCCTTGG others(3): Show |
G | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.790+224_790+233del others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17772964 | |||||||
chr19:17773311 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.790+570C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773311 | |||||||
chr19:17773406 | T | G | 1 | a0001c0009t0002g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.790+665T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773406 | |||||||
chr19:17773643 | C | T | 1 | a0001c0001t0005g0198 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.791-596C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773643 | |||||||
chr19:17773764 | G | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.791-475G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773764 | |||||||
chr19:17773901 | CTCT | C | 12 | a0001c0002t0001g0151 a0001c0003t0001g0008 a0001c0003t0001g0019 others(9): Show |
13 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.791-336_791-334del others(3): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 17773901 | ||||||
chr19:17773903 | CT | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0249 a0001c0001t0001g0271 others(40): Show |
45 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.791-320delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 17773903 | ||||||
chr19:17773903 | CTT | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.791-321_791-320del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 17773903 | ||||||
chr19:17773904 | T | TC | 22 | a0001c0002t0002g0049 a0001c0002t0002g0066 a0001c0002t0002g0067 others(19): Show |
23 | HG00140.hp2 HG00741.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.791-335_791-334ins others(1): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773904 | |||||||
chr19:17773905 | T | C | 3 | a0001c0001t0001g0267 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG03831.hp2 HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.791-334T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773905 | |||||||
chr19:17773996 | C | T | 1 | a0001c0002t0001g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.791-243C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773996 | |||||||
chr19:17774036 | C | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.791-203C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17774036 | |||||||
chr19:17774072 | G | A | 43 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 others(40): Show |
44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.791-167G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17774072 | |||||||
chr19:17774499 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.920+21G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774499 | |||||||
chr19:17774516 | A | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.920+38A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774516 | |||||||
chr19:17774527 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.920+49C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774527 | |||||||
chr19:17774730 | G | A | 2 | a0001c0003t0001g0144 a0001c0012t0001g0145 |
2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.920+252G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774730 | |||||||
chr19:17774846 | C | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(17): Show |
21 | HG01175.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.921-210C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774846 | |||||||
chr19:17774890 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0223 a0001c0001t0001g0241 others(3): Show |
7 | HG00609.hp2 HG00673.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.921-166A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774890 | |||||||
chr19:17775019 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.921-37C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17775019 | |||||||
chr19:17775213 | G | A | 5 | a0001c0003t0001g0167 a0001c0007t0002g0142 a0001c0007t0002g0328 others(2): Show |
5 | HG01123.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.945+133G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 14/28 | chr19 | 17775213 | |||||||
chr19:17775253 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0306 |
2 | NA18965.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.945+173C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 14/28 | chr19 | 17775253 | |||||||
chr19:17775447 | C | T | 1 | a0001c0006t0001g0182 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.946-9C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 14/28 | chr19 | 17775447 | |||||||
chr19:17775741 | G | T | 3 | a0001c0001t0001g0258 a0001c0001t0001g0300 a0001c0001t0001g0302 |
3 | HG00280.hp1 HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1003+228G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/28 | chr19 | 17775741 | |||||||
chr19:17775810 | G | C | 6 | a0001c0001t0001g0181 a0001c0001t0001g0218 a0001c0001t0001g0220 others(3): Show |
6 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1004-173G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/28 | chr19 | 17775810 | |||||||
chr19:17775857 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1004-126G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/28 | chr19 | 17775857 | |||||||
chr19:17775885 | C | T | 1 | a0001c0011t0002g0063 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1004-98C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/28 | chr19 | 17775885 | |||||||
chr19:17775943 | G | A | 17 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(14): Show |
17 | HG00544.hp2 HG01192.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1004-40G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/28 | chr19 | 17775943 | |||||||
chr19:17776181 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1182+20C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 16/28 | chr19 | 17776181 | |||||||
chr19:17776215 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1183-32T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 16/28 | chr19 | 17776215 | |||||||
chr19:17776235 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183-12C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 16/28 | chr19 | 17776235 | |||||||
chr19:17776511 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1208-124C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 17/28 | chr19 | 17776511 | |||||||
chr19:17776550 | C | T | 1 | a0001c0002t0001g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1208-85C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 17/28 | chr19 | 17776550 | |||||||
chr19:17776754 | G | A | 75 | a0001c0002t0001g0151 a0001c0002t0002g0049 a0001c0002t0002g0066 others(72): Show |
78 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1259+68G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17776754 | |||||||
chr19:17776799 | G | GT | 11 | a0001c0001t0001g0071 a0001c0001t0001g0199 a0001c0001t0001g0301 others(8): Show |
11 | HG01934.hp1 HG02559.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1259+120dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17776799 | ||||||
chr19:17776999 | T | C | 2 | a0001c0003t0001g0168 a0001c0003t0001g0169 |
2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1259+313T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17776999 | |||||||
chr19:17777061 | G | T | 1 | a0001c0001t0001g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1259+375G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777061 | |||||||
chr19:17777067 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1259+381G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777067 | |||||||
chr19:17777177 | T | A | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+491T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777177 | |||||||
chr19:17777179 | G | T | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+493G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777179 | |||||||
chr19:17777181 | G | T | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+495G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777181 | |||||||
chr19:17777185 | G | C | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+499G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777185 | |||||||
chr19:17777186 | G | A | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+500G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777186 | |||||||
chr19:17777188 | T | G | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+502T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777188 | |||||||
chr19:17777201 | C | G | 6 | a0001c0006t0001g0171 a0001c0006t0001g0172 a0001c0006t0001g0173 others(3): Show |
6 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1259+515C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777201 | |||||||
chr19:17777226 | T | G | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+540T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777226 | |||||||
chr19:17777227 | G | T | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+541G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777227 | |||||||
chr19:17777228 | A | C | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+542A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777228 | |||||||
chr19:17777237 | T | A | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+551T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777237 | |||||||
chr19:17777245 | T | C | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+559T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777245 | |||||||
chr19:17777263 | G | C | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+577G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777263 | |||||||
chr19:17777264 | T | A | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+578T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777264 | |||||||
chr19:17777265 | G | A | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+579G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777265 | |||||||
chr19:17777297 | G | A | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+611G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777297 | |||||||
chr19:17777303 | A | G | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+617A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777303 | |||||||
chr19:17777308 | A | T | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+622A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777308 | |||||||
chr19:17777311 | C | G | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+625C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777311 | |||||||
chr19:17777312 | G | C | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+626G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777312 | |||||||
chr19:17777327 | G | A | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+641G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777327 | |||||||
chr19:17777328 | A | G | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+642A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777328 | |||||||
chr19:17777345 | T | G | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+659T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777345 | |||||||
chr19:17777355 | A | G | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+669A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777355 | |||||||
chr19:17777366 | A | G | 1 | a0009c0019t0001g0320 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+680A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777366 | |||||||
chr19:17777405 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1259+719A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777405 | |||||||
chr19:17777512 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1260-625G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777512 | |||||||
chr19:17777535 | CA | C | 91 | a0001c0002t0001g0057 a0001c0002t0001g0058 a0001c0002t0001g0081 others(88): Show |
94 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1260-575delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17777535 | ||||||
chr19:17777535 | CAAA | C | 25 | a0001c0001t0001g0065 a0001c0001t0001g0114 a0001c0001t0001g0199 others(22): Show |
25 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.1260-577_1260-575d others(5): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17777535 | ||||||
chr19:17777535 | CAAAA | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1260-578_1260-575d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17777535 | ||||||
chr19:17777535 | CAAAAA | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(12): Show |
16 | HG01175.hp1 HG01255.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1260-579_1260-575d others(7): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17777535 | ||||||
chr19:17777535 | CAAAAAA | C | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1260-580_1260-575d others(8): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17777535 | ||||||
chr19:17777551 | A | G | 72 | a0001c0002t0001g0151 a0001c0002t0002g0049 a0001c0002t0002g0066 others(69): Show |
75 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1260-586A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777551 | |||||||
chr19:17777845 | G | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(260): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1260-292G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777845 | |||||||
chr19:17777854 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1260-283C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777854 | |||||||
chr19:17777970 | C | T | 1 | a0001c0001t0005g0259 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1260-167C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777970 | |||||||
chr19:17777978 | G | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(165): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1260-159G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777978 | |||||||
chr19:17777986 | C | T | 1 | a0001c0002t0002g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1260-151C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777986 | |||||||
chr19:17778017 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1260-120C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17778017 | |||||||
chr19:17778038 | C | CA | 75 | a0001c0001t0001g0059 a0001c0002t0001g0151 a0001c0002t0002g0049 others(72): Show |
78 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1260-87dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17778038 | ||||||
chr19:17778235 | G | A | 28 | a0001c0002t0001g0151 a0001c0003t0001g0007 a0001c0003t0001g0008 others(25): Show |
30 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(27): Show |
splice_region_variant&intron_variant | LOW | c.1351+7G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 19/28 | chr19 | 17778235 | |||||||
chr19:17778350 | A | G | 1 | a0001c0004t0003g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1351+122A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 19/28 | chr19 | 17778350 | |||||||
chr19:17778977 | G | C | 4 | a0001c0002t0002g0066 a0001c0002t0002g0067 a0001c0003t0001g0168 others(1): Show |
4 | HG02109.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+93G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17778977 | |||||||
chr19:17779036 | G | A | 1 | a0001c0012t0001g0145 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1627+152G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779036 | |||||||
chr19:17779054 | C | CG | 38 | a0001c0001t0001g0073 a0001c0001t0001g0097 a0001c0001t0001g0154 others(35): Show |
38 | HG00609.hp2 HG01175.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.1627+172dupG | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779054 | ||||||
chr19:17779269 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1627+385A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779269 | |||||||
chr19:17779270 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(256): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1627+386A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779270 | |||||||
chr19:17779378 | T | C | 5 | a0001c0003t0001g0167 a0001c0007t0002g0142 a0001c0007t0002g0328 others(2): Show |
5 | HG01123.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1627+494T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779378 | |||||||
chr19:17779382 | G | A | 1 | a0001c0003t0001g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1627+498G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779382 | |||||||
chr19:17779506 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 |
3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1627+622G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779506 | |||||||
chr19:17779515 | G | T | 1 | a0002c0018t0001g0294 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1627+631G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779515 | |||||||
chr19:17779545 | A | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(260): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1627+661A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779545 | |||||||
chr19:17779613 | A | AGCGGAGT others(327): Show |
2 | a0001c0003t0001g0144 a0001c0012t0001g0145 |
2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1627+763_1627+764i others(336): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779613 | ||||||
chr19:17779613 | AGCGGAGT others(27): Show |
A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(21): Show |
25 | HG01123.hp2 HG01175.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1627+764_1627+797d others(36): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779613 | ||||||
chr19:17779625 | G | GGAGGGAG others(89): Show |
1 | a0001c0005t0001g0121 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1627+742_1627+837d others(98): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779625 | ||||||
chr19:17779648 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1627+764G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779648 | |||||||
chr19:17779651 | G | GAGTCAAG others(25): Show |
1 | a0001c0001t0001g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1627+798_1627+829d others(34): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779651 | ||||||
chr19:17779721 | CAAGG | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1627+838_1627+841d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779721 | |||||||
chr19:17779952 | T | TG | 34 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0087 others(31): Show |
34 | HG00544.hp2 HG01099.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1627+1074dupG | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779952 | ||||||
chr19:17780011 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(152): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1627+1127G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780011 | |||||||
chr19:17780156 | A | C | 1 | a0001c0003t0004g0148 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1628-1075A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780156 | |||||||
chr19:17780161 | C | CT | 222 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(219): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1628-1050dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17780161 | ||||||
chr19:17780161 | C | CTT | 14 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0154 others(11): Show |
14 | HG00140.hp2 HG00741.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-1051_1628-105 others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17780161 | ||||||
chr19:17780161 | C | T | 1 | a0001c0005t0001g0115 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1628-1070C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780161 | |||||||
chr19:17780207 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1628-1024C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780207 | |||||||
chr19:17780208 | G | A | 1 | a0001c0003t0001g0207 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1628-1023G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780208 | |||||||
chr19:17780272 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(256): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1628-959T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780272 | |||||||
chr19:17780323 | G | A | 2 | a0001c0007t0002g0328 a0001c0007t0003g0327 |
2 | HG01123.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1628-908G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780323 | |||||||
chr19:17780453 | C | T | 1 | a0001c0012t0001g0145 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1628-778C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780453 | |||||||
chr19:17780567 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1628-664C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780567 | |||||||
chr19:17780687 | C | T | 3 | a0001c0002t0001g0088 a0001c0002t0001g0090 a0001c0002t0001g0099 |
3 | HG03516.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-544C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780687 | |||||||
chr19:17780750 | T | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(256): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1628-481T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780750 | |||||||
chr19:17780959 | C | T | 2 | a0001c0003t0001g0157 a0001c0003t0004g0149 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1628-272C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780959 | |||||||
chr19:17781356 | G | A | 2 | a0001c0002t0002g0066 a0001c0002t0002g0067 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1740+13G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 21/28 | chr19 | 17781356 | |||||||
chr19:17781357 | C | A | 2 | a0001c0002t0002g0066 a0001c0002t0002g0067 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1740+14C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 21/28 | chr19 | 17781357 | |||||||
chr19:17781384 | G | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1740+41G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 21/28 | chr19 | 17781384 | |||||||
chr19:17781564 | G | A | 15 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0084 others(12): Show |
16 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1828+25G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 22/28 | chr19 | 17781564 | |||||||
chr19:17781635 | C | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0003t0001g0167 others(4): Show |
7 | HG01123.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1829-77C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 22/28 | chr19 | 17781635 | |||||||
chr19:17781669 | A | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1829-43A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 22/28 | chr19 | 17781669 | |||||||
chr19:17781680 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1829-32G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 22/28 | chr19 | 17781680 | |||||||
chr19:17781897 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1937+77C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17781897 | |||||||
chr19:17781987 | CT | C | 62 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0002t0001g0057 others(59): Show |
64 | HG00639.hp2 HG01069.hp2 HG01167.hp1 others(61): Show |
intron_variant | MODIFIER | c.1937+196delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | 17781987 | ||||||
chr19:17781987 | CTT | C | 35 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0003t0001g0167 others(32): Show |
36 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.1937+195_1937+196d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | 17781987 | ||||||
chr19:17781987 | CTTTT | C | 9 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0053 others(6): Show |
9 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1937+193_1937+196d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | 17781987 | ||||||
chr19:17781987 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0224 |
2 | HG01981.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1937+182_1937+196d others(17): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | 17781987 | ||||||
chr19:17781987 | CTTTTTTT others(9): Show |
C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(197): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1937+181_1937+196d others(18): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | 17781987 | ||||||
chr19:17782071 | G | A | 215 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(212): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1937+251G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782071 | |||||||
chr19:17782103 | G | A | 6 | a0001c0006t0001g0171 a0001c0006t0001g0172 a0001c0006t0001g0173 others(3): Show |
6 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1937+283G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782103 | |||||||
chr19:17782328 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(57): Show |
62 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1937+508G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782328 | |||||||
chr19:17782371 | A | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1937+551A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782371 | |||||||
chr19:17782528 | A | G | 2 | a0001c0003t0001g0162 a0001c0003t0004g0148 |
2 | HG01517.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1938-489A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782528 | |||||||
chr19:17782565 | A | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1938-452A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782565 | |||||||
chr19:17782679 | A | C | 27 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0019 others(24): Show |
29 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1938-338A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782679 | |||||||
chr19:17782793 | A | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(57): Show |
62 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1938-224A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782793 | |||||||
chr19:17782814 | T | A | 1 | a0001c0001t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1938-203T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782814 | |||||||
chr19:17783185 | G | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0184 a0001c0001t0001g0186 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2093+13G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783185 | |||||||
chr19:17783247 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2093+75C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783247 | |||||||
chr19:17783259 | A | AT | 43 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0084 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2093+93dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 17783259 | ||||||
chr19:17783259 | A | ATT | 3 | a0001c0003t0001g0007 a0001c0003t0001g0159 a0001c0003t0001g0207 |
4 | HG01167.hp2 HG02738.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.2093+92_2093+93dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 17783259 | ||||||
chr19:17783266 | C | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2093+94C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783266 | |||||||
chr19:17783271 | C | T | 1 | a0001c0003t0002g0048 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2093+99C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783271 | |||||||
chr19:17783441 | G | A | 2 | a0001c0002t0006g0185 a0001c0002t0006g0191 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2093+269G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783441 | |||||||
chr19:17783460 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2093+288G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783460 | |||||||
chr19:17783488 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.2093+316A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783488 | |||||||
chr19:17783506 | A | G | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2093+334A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783506 | |||||||
chr19:17783563 | C | T | 3 | a0001c0002t0001g0179 a0001c0002t0001g0245 a0001c0002t0001g0253 |
3 | HG01256.hp2 HG02273.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2093+391C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783563 | |||||||
chr19:17784032 | G | T | 1 | a0001c0001t0001g0252 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2094-71G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17784032 | |||||||
chr19:17784069 | C | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0053 others(35): Show |
40 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2094-34C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17784069 | |||||||
chr19:17784413 | C | T | 1 | a0001c0002t0001g0123 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2226+178C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 25/28 | chr19 | 17784413 | |||||||
chr19:17784442 | G | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2226+207G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 25/28 | chr19 | 17784442 | |||||||
chr19:17784471 | A | C | 222 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(219): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2226+236A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 25/28 | chr19 | 17784471 | |||||||
chr19:17784550 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2227-175C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 25/28 | chr19 | 17784550 | |||||||
chr19:17784631 | G | A | 2 | a0001c0002t0001g0245 a0001c0003t0001g0144 |
2 | HG02273.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2227-94G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 25/28 | chr19 | 17784631 | |||||||
chr19:17784981 | C | A | 3 | a0001c0001t0001g0335 a0001c0002t0002g0066 a0001c0002t0002g0067 |
3 | HG02109.hp1 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2426+57C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17784981 | |||||||
chr19:17785017 | G | A | 34 | a0001c0001t0001g0056 a0001c0001t0001g0061 a0001c0001t0001g0062 others(31): Show |
34 | HG00280.hp1 HG00609.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2426+93G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785017 | |||||||
chr19:17785065 | G | A | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(123): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2426+141G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785065 | |||||||
chr19:17785242 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2426+318T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785242 | |||||||
chr19:17785341 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2426+417C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785341 | |||||||
chr19:17785423 | A | G | 6 | a0001c0002t0001g0093 a0001c0002t0001g0129 a0001c0002t0001g0130 others(3): Show |
6 | NA18963.hp1 NA18985.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.2426+499A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785423 | |||||||
chr19:17785483 | A | G | 37 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0209 others(34): Show |
38 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.2426+559A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785483 | |||||||
chr19:17785518 | C | T | 1 | a0001c0003t0001g0144 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2426+594C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785518 | |||||||
chr19:17785533 | AT | A | 6 | a0001c0001t0001g0077 a0001c0002t0001g0095 a0001c0002t0001g0096 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2426+610delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785533 | |||||||
chr19:17785555 | C | T | 6 | a0001c0002t0001g0092 a0001c0002t0001g0122 a0001c0002t0001g0123 others(3): Show |
6 | NA18945.hp2 NA18957.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.2426+631C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785555 | |||||||
chr19:17785556 | G | A | 1 | a0001c0016t0001g0235 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2426+632G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785556 | |||||||
chr19:17785562 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2426+638G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785562 | |||||||
chr19:17785615 | C | T | 4 | a0001c0001t0001g0265 a0001c0003t0001g0157 a0001c0003t0004g0149 others(1): Show |
4 | HG01168.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2426+691C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785615 | |||||||
chr19:17785636 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2426+712A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785636 | |||||||
chr19:17785753 | G | A | 6 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0186 others(3): Show |
6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2427-821G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785753 | |||||||
chr19:17785833 | C | CA | 94 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0055 others(91): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.2427-726dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17785833 | ||||||
chr19:17785833 | C | CAA | 32 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0068 others(29): Show |
33 | HG00733.hp2 HG01168.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.2427-727_2427-726d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17785833 | ||||||
chr19:17785833 | C | CAAA | 10 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0051 others(7): Show |
10 | HG01981.hp1 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2427-728_2427-726d others(5): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17785833 | ||||||
chr19:17785833 | CA | C | 7 | a0001c0001t0001g0199 a0001c0001t0001g0252 a0001c0001t0001g0282 others(4): Show |
7 | HG01257.hp2 HG01975.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.2427-726delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17785833 | ||||||
chr19:17785935 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2427-639G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785935 | |||||||
chr19:17785978 | T | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
41 | HG00733.hp2 HG01168.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.2427-596T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785978 | |||||||
chr19:17785979 | A | T | 57 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0170 others(54): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.2427-595A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785979 | |||||||
chr19:17785980 | A | T | 1 | a0001c0003t0001g0152 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2427-594A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785980 | |||||||
chr19:17786016 | T | C | 24 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0280 others(21): Show |
26 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2427-558T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17786016 | |||||||
chr19:17786048 | A | G | 1 | a0001c0007t0002g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2427-526A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17786048 | |||||||
chr19:17786091 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2427-483T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17786091 | |||||||
chr19:17786331 | TCAAAAAA others(5): Show |
T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0070 others(26): Show |
30 | HG00738.hp1 HG00741.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.2427-230_2427-219d others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17786331 | ||||||
chr19:17786361 | A | AAC | 3 | a0001c0001t0001g0272 a0001c0001t0001g0275 a0001c0001t0001g0281 |
3 | HG03017.hp1 NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2427-191_2427-190d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17786361 | ||||||
chr19:17786361 | AAC | A | 68 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(65): Show |
71 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.2427-191_2427-190d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17786361 | ||||||
chr19:17786361 | AACAC | A | 3 | a0001c0002t0002g0066 a0001c0002t0002g0067 a0005c0010t0002g0143 |
3 | HG02109.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2427-193_2427-190d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17786361 | ||||||
chr19:17786461 | A | T | 1 | a0001c0002t0001g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2427-113A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17786461 | |||||||
chr19:17787175 | G | T | 1 | a0001c0003t0001g0144 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2483-507G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787175 | |||||||
chr19:17787187 | G | A | 34 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0209 others(31): Show |
35 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2483-495G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787187 | |||||||
chr19:17787223 | C | CA | 65 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0079 others(62): Show |
65 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2483-429dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | ||||||
chr19:17787223 | C | CAA | 15 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0085 others(12): Show |
15 | HG00280.hp1 HG00423.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2483-430_2483-429d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | ||||||
chr19:17787223 | CA | C | 8 | a0001c0001t0001g0156 a0001c0001t0001g0262 a0001c0001t0001g0284 others(5): Show |
8 | HG00323.hp1 HG02040.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2483-429delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | ||||||
chr19:17787223 | CAA | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(11): Show |
15 | HG01175.hp1 HG01891.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.2483-430_2483-429d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | ||||||
chr19:17787223 | CAAA | C | 67 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0053 others(64): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.2483-431_2483-429d others(5): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | ||||||
chr19:17787223 | CAAAA | C | 6 | a0001c0001t0001g0265 a0001c0002t0001g0088 a0001c0002t0001g0099 others(3): Show |
6 | HG01168.hp2 HG01256.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2483-432_2483-429d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | ||||||
chr19:17787223 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0137 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2483-438_2483-429d others(12): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | ||||||
chr19:17787223 | CAAAAAAA others(4): Show |
C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0070 others(25): Show |
29 | HG00738.hp1 HG00741.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2483-439_2483-429d others(13): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | ||||||
chr19:17787242 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2483-440A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787242 | |||||||
chr19:17787402 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2483-280C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787402 | |||||||
chr19:17787411 | T | TA | 42 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0070 others(39): Show |
43 | HG00438.hp1 HG00438.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.2483-254dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787411 | ||||||
chr19:17787411 | TA | T | 7 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0271 others(4): Show |
7 | HG01099.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2483-254delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787411 | ||||||
chr19:17787412 | A | G | 2 | a0001c0001t0001g0324 a0001c0002t0001g0098 |
2 | HG02622.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2483-270A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787412 | |||||||
chr19:17787658 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
7 | HG01891.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2483-24G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787658 | |||||||
chr19:17787908 | G | A | 27 | a0001c0001t0001g0078 a0001c0001t0001g0212 a0001c0001t0001g0213 others(24): Show |
29 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.2647+62G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17787908 | |||||||
chr19:17787953 | G | A | 1 | a0001c0003t0001g0207 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2647+107G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17787953 | |||||||
chr19:17787981 | A | T | 9 | a0001c0003t0007g0150 a0001c0003t0007g0164 a0001c0004t0003g0020 others(6): Show |
9 | HG00733.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2647+135A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17787981 | |||||||
chr19:17788077 | G | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0254 a0001c0002t0001g0112 |
3 | HG03491.hp2 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2648-207G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788077 | |||||||
chr19:17788221 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2648-63G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788221 | |||||||
chr19:17788238 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2648-46G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788238 | |||||||
chr19:17788242 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2648-42C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788242 | |||||||
chr19:17788271 | T | C | 3 | a0001c0004t0003g0020 a0001c0004t0003g0021 a0001c0007t0003g0327 |
3 | HG01884.hp2 HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2648-13T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788271 | |||||||
chr19:17788277 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp2 | splice_region_variant&intron_variant | LOW | c.2648-7C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788277 |