Item | Value |
---|---|
geneid | 2339 |
ensemblid | ENSG00000168522.13 |
hgncid | 3782 |
symbol | FNTA |
name | farnesyltransferase, CAAX box, alpha |
refseq_nuc | NM_002027.3 |
refseq_prot | NP_002018.1 |
ensembl_nuc | ENST00000302279.8 |
ensembl_prot | ENSP00000303423.3 |
mane_status | MANE Select |
chr | chr8 |
start | 43056323 |
end | 43085785 |
strand | + |
ver | v1.2 |
region | chr8:43056323-43085785 |
region5000 | chr8:43051323-43090785 |
regionname0 | FNTA_chr8_43056323_43085785 |
regionname5000 | FNTA_chr8_43051323_43090785 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 379 | 293 | 87 | 54 | 100 | 16 | 34 | 66 | FNTA_chr8_43051323_43090785 | FNTA | MAATE others(374): Show |
chr8 | 43051323 | 43090785 |
a0002 | 0/0 | 379 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | MAATE others(374): Show |
chr8 | 43051323 | 43090785 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1137 | 275 | 71 | 53 | 100 | 16 | 33 | FNTA_chr8_43051323_43090785 | FNTA | ATGGC others(1132): Show |
chr8 | 43051323 | 43090785 | ||
a0001c0002 | 0/0 | 1137 | 16 | 15 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | ATGGC others(1132): Show |
chr8 | 43051323 | 43090785 | ||
a0001c0003 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | ATGGC others(1132): Show |
chr8 | 43051323 | 43090785 | ||
a0001c0005 | 0/0 | 1137 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | ATGGC others(1132): Show |
chr8 | 43051323 | 43090785 | ||
a0002c0004 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | ATGGC others(1132): Show |
chr8 | 43051323 | 43090785 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1667 | 273 | 69 | 53 | 100 | 16 | 33 | FNTA_chr8_43051323_43090785 | FNTA | ACCTC others(1662): Show |
chr8 | 43051323 | 43090785 |
a0001c0001t0002 | 0/0 | 1667 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | ACCTC others(1662): Show |
chr8 | 43051323 | 43090785 |
a0001c0001t0003 | 0/0 | 1667 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | ACCTC others(1662): Show |
chr8 | 43051323 | 43090785 |
a0001c0002t0001 | 0/0 | 1667 | 16 | 15 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | ACCTC others(1662): Show |
chr8 | 43051323 | 43090785 |
a0001c0003t0001 | 0/0 | 1667 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | ACCTC others(1662): Show |
chr8 | 43051323 | 43090785 |
a0001c0005t0001 | 0/0 | 1667 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | ACCTC others(1662): Show |
chr8 | 43051323 | 43090785 |
a0002c0004t0001 | 0/0 | 1667 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | ACCTC others(1662): Show |
chr8 | 43051323 | 43090785 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 23 | 13 | 1 | 6 | 2 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0002 | 0/0 | 11 | 1 | 2 | 4 | 0 | 4 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0004 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0007 | 0/0 | 6 | 4 | 0 | 2 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0011 | 1/0 | 4 | 2 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0002t0001g0003 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0001c0005t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
a0002c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02647 | hp2 | a0002 | c0004 | t0001 | g0158 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0192 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG04228 | hp1 | a0001 | c0005 | t0001 | g0022 | SAS | STU | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | YRI | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | YRI | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ASW | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | USA | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0047 | REF | REF | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | FNTA_chr8_43051323_43090785 | FNTA | chr8 | 43051323 | 43090785 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:43056468 | C | T | 1 | a0002 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.122C>T | p.Ala41Val | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/9 | 146/1667 | 122/1140 | 41/379 | chr8 | 43056468 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:43056412 | C | G | 1 | a0001c0005 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.66C>G | p.Pro22Pro | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/9 | 90/1667 | 66/1140 | 22/379 | chr8 | 43056412 | |||
chr8:43069654 | A | G | 1 | a0001c0003 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.501A>G | p.Gln167Gln | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/9 | 525/1667 | 501/1140 | 167/379 | chr8 | 43069654 | |||
chr8:43084791 | C | A | 1 | a0001c0002 | 16 | HG01243.hp1 HG02109.hp1 HG02615.hp1 others(13): Show |
synonymous_variant | LOW | c.927C>A | p.Pro309Pro | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 8/9 | 951/1667 | 927/1140 | 309/379 | chr8 | 43084791 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:43085397 | G | A | 1 | a0001c0001t0002 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 9/9 | 115 | chr8 | 43085397 | ||||||
chr8:43085506 | A | G | 1 | a0001c0001t0003 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 9/9 | 224 | chr8 | 43085506 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:43056630 | C | T | 1 | a0001c0003t0001g0192 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.200+84C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43056630 | |||||||
chr8:43056697 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.200+151G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43056697 | |||||||
chr8:43056701 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.200+155G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43056701 | |||||||
chr8:43056843 | T | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(33): Show |
58 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.200+297T>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43056843 | |||||||
chr8:43056846 | G | C | 5 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0068 others(2): Show |
13 | HG01243.hp1 HG02615.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.200+300G>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43056846 | |||||||
chr8:43056864 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.200+318C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43056864 | |||||||
chr8:43056961 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.200+415G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43056961 | |||||||
chr8:43057105 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.200+559C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43057105 | |||||||
chr8:43057150 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.200+604G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43057150 | |||||||
chr8:43057215 | A | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0187 others(4): Show |
10 | HG00140.hp1 HG00642.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.200+669A>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43057215 | |||||||
chr8:43057383 | T | C | 1 | a0001c0001t0001g0019 | 2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.200+837T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43057383 | |||||||
chr8:43057427 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG02055.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.200+881C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43057427 | |||||||
chr8:43057435 | T | C | 14 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(11): Show |
22 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.200+889T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43057435 | |||||||
chr8:43057538 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.200+992G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43057538 | |||||||
chr8:43057563 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.200+1017C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43057563 | |||||||
chr8:43057949 | T | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0081 |
3 | NA18997.hp2 NA19000.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.201-1143T>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43057949 | |||||||
chr8:43057956 | C | CA | 12 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0001g0082 others(9): Show |
15 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.201-1119dupA | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 43057956 | ||||||
chr8:43058028 | G | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-1064G>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43058028 | |||||||
chr8:43058121 | G | A | 1 | a0001c0003t0001g0192 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.201-971G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43058121 | |||||||
chr8:43058372 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.201-720A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43058372 | |||||||
chr8:43058542 | C | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-550C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43058542 | |||||||
chr8:43058898 | A | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02280.hp2 HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.201-194A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 1/8 | chr8 | 43058898 | |||||||
chr8:43059207 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.286+30G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43059207 | |||||||
chr8:43059322 | T | A | 1 | a0001c0001t0001g0019 | 2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.286+145T>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43059322 | |||||||
chr8:43059482 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.286+305A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43059482 | |||||||
chr8:43059556 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0091 a0001c0001t0001g0174 others(3): Show |
8 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+379A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43059556 | |||||||
chr8:43059565 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.286+388C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43059565 | |||||||
chr8:43059805 | AT | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(146): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.286+636delT | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43059805 | ||||||
chr8:43060276 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.286+1099A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43060276 | |||||||
chr8:43060490 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.286+1313C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43060490 | |||||||
chr8:43060495 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG01516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.286+1318C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43060495 | |||||||
chr8:43060530 | C | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+1353C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43060530 | |||||||
chr8:43060626 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.286+1449G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43060626 | |||||||
chr8:43060675 | C | CA | 6 | a0001c0001t0001g0013 a0001c0001t0001g0148 a0001c0001t0001g0183 others(3): Show |
8 | HG01192.hp2 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+1516dupA | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43060675 | ||||||
chr8:43060675 | CAAAA | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.286+1513_286+1516d others(6): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43060675 | ||||||
chr8:43060713 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.286+1536C>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43060713 | |||||||
chr8:43061177 | A | C | 7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+2000A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43061177 | |||||||
chr8:43061271 | G | T | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.286+2094G>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43061271 | |||||||
chr8:43061279 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.286+2102C>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43061279 | |||||||
chr8:43061435 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.286+2258T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43061435 | |||||||
chr8:43061652 | A | G | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-2449A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43061652 | |||||||
chr8:43061695 | T | A | 33 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0071 others(30): Show |
44 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.287-2406T>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43061695 | |||||||
chr8:43061724 | AT | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
11 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-2365delT | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43061724 | ||||||
chr8:43061796 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.287-2305C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43061796 | |||||||
chr8:43061798 | C | T | 1 | a0001c0003t0001g0192 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.287-2303C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43061798 | |||||||
chr8:43061799 | G | A | 1 | a0001c0001t0003g0102 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.287-2302G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43061799 | |||||||
chr8:43061829 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.287-2272C>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43061829 | |||||||
chr8:43062152 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.287-1949A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43062152 | |||||||
chr8:43062173 | A | ATG | 16 | a0001c0001t0001g0033 a0001c0001t0001g0071 a0001c0001t0001g0072 others(13): Show |
25 | HG00438.hp2 HG01074.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-1900_287-1899d others(4): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43062173 | ||||||
chr8:43062173 | A | ATGTG | 12 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0083 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.287-1902_287-1899d others(6): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43062173 | ||||||
chr8:43062173 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0019 | 2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.287-1908_287-1899d others(12): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43062173 | ||||||
chr8:43062173 | ATG | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0060 others(7): Show |
12 | HG00140.hp2 HG00621.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.287-1900_287-1899d others(4): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43062173 | ||||||
chr8:43062173 | ATGTG | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.287-1902_287-1899d others(6): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43062173 | ||||||
chr8:43062225 | C | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.287-1876C>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43062225 | |||||||
chr8:43062249 | T | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.287-1852T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43062249 | |||||||
chr8:43062533 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.287-1568C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43062533 | |||||||
chr8:43062860 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.287-1241A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43062860 | |||||||
chr8:43063054 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.287-1047A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063054 | |||||||
chr8:43063086 | C | A | 2 | a0001c0001t0002g0080 a0001c0002t0001g0079 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.287-1015C>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063086 | |||||||
chr8:43063087 | C | CT | 11 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0059 others(8): Show |
18 | HG00673.hp1 HG01175.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.287-996dupT | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43063087 | ||||||
chr8:43063087 | CT | C | 20 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0071 others(17): Show |
29 | HG00558.hp2 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.287-996delT | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43063087 | ||||||
chr8:43063125 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.287-976A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063125 | |||||||
chr8:43063270 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.287-831G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063270 | |||||||
chr8:43063315 | A | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.287-786A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063315 | |||||||
chr8:43063380 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0058 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.287-721C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063380 | |||||||
chr8:43063477 | G | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-624G>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063477 | |||||||
chr8:43063508 | TTAA | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-588_287-586del others(3): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 43063508 | ||||||
chr8:43063678 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.287-423T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063678 | |||||||
chr8:43063747 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.287-354A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063747 | |||||||
chr8:43063846 | T | G | 1 | a0001c0001t0003g0102 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.287-255T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063846 | |||||||
chr8:43063867 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.287-234A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063867 | |||||||
chr8:43063903 | T | G | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02451.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.287-198T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43063903 | |||||||
chr8:43064086 | G | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-15G>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 2/8 | chr8 | 43064086 | |||||||
chr8:43064274 | CTTTTTTT others(14): Show |
C | 1 | a0001c0002t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.401+80_401+100delA others(20): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43064274 | ||||||
chr8:43064315 | AT | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.401+108delT | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43064315 | ||||||
chr8:43064348 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.401+133G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43064348 | |||||||
chr8:43064567 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.401+352G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43064567 | |||||||
chr8:43064815 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.401+600A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43064815 | |||||||
chr8:43065205 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.401+990A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43065205 | |||||||
chr8:43065238 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.401+1023A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43065238 | |||||||
chr8:43065499 | AGCCTCCC others(1005): Show |
A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0091 a0001c0001t0001g0174 others(4): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.401+1297_401+2308d others(2): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43065499 | ||||||
chr8:43065542 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.401+1327C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43065542 | |||||||
chr8:43065628 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.401+1413G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43065628 | |||||||
chr8:43065776 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.401+1561C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43065776 | |||||||
chr8:43065955 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.401+1740C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43065955 | |||||||
chr8:43066071 | T | G | 1 | a0001c0001t0001g0007 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.401+1856T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066071 | |||||||
chr8:43066117 | A | G | 1 | a0001c0005t0001g0022 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.401+1902A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066117 | |||||||
chr8:43066171 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.401+1956C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066171 | |||||||
chr8:43066262 | C | CT | 7 | a0001c0001t0001g0059 a0001c0001t0001g0082 a0001c0001t0001g0083 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.401+2059dupT | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43066262 | ||||||
chr8:43066288 | G | A | 1 | a0001c0002t0001g0077 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.401+2073G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066288 | |||||||
chr8:43066291 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.401+2076C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066291 | |||||||
chr8:43066346 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.401+2131T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066346 | |||||||
chr8:43066381 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0001g0166 others(1): Show |
8 | HG00673.hp1 HG02523.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.401+2166C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066381 | |||||||
chr8:43066510 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG02886.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.401+2295C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066510 | |||||||
chr8:43066587 | C | CGT | 8 | a0001c0001t0001g0029 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.401+2397_401+2398d others(4): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43066587 | ||||||
chr8:43066587 | C | CGTGT | 5 | a0001c0001t0001g0128 a0001c0001t0001g0170 a0001c0001t0001g0183 others(2): Show |
5 | HG02109.hp1 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.401+2395_401+2398d others(6): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43066587 | ||||||
chr8:43066587 | C | CGTGTGT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(83): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.401+2393_401+2398d others(8): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43066587 | ||||||
chr8:43066587 | C | CGTGTGTG others(1): Show |
39 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0038 others(36): Show |
56 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.401+2391_401+2398d others(10): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43066587 | ||||||
chr8:43066587 | C | CGTGTGTG others(3): Show |
8 | a0001c0001t0001g0019 a0001c0001t0001g0095 a0001c0001t0001g0105 others(5): Show |
9 | HG01261.hp1 HG01884.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.401+2389_401+2398d others(12): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43066587 | ||||||
chr8:43066587 | C | CGTGTGTG others(5): Show |
6 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.401+2387_401+2398d others(14): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43066587 | ||||||
chr8:43066587 | C | CGTGTGTG others(7): Show |
1 | a0001c0001t0001g0071 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.401+2385_401+2398d others(16): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43066587 | ||||||
chr8:43066613 | T | TGTGTGTG | 3 | a0001c0001t0001g0062 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG02056.hp1 NA19000.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.401+2398_401+2399i others(9): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066613 | |||||||
chr8:43066686 | G | C | 1 | a0001c0001t0001g0019 | 2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.401+2471G>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066686 | |||||||
chr8:43066745 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
6 | HG01192.hp2 HG01884.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.401+2530C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43066745 | |||||||
chr8:43067000 | A | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.402-2555A>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43067000 | |||||||
chr8:43067272 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.402-2283A>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43067272 | |||||||
chr8:43067422 | C | T | 2 | a0001c0002t0001g0077 a0001c0002t0001g0078 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.402-2133C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43067422 | |||||||
chr8:43067580 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.402-1975G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43067580 | |||||||
chr8:43067646 | C | CT | 17 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0072 others(14): Show |
26 | HG01243.hp1 HG01261.hp1 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.402-1894dupT | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 43067646 | ||||||
chr8:43067697 | T | C | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.402-1858T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43067697 | |||||||
chr8:43067749 | TC | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0091 a0001c0001t0001g0174 others(4): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.402-1805delC | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43067749 | |||||||
chr8:43067781 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.402-1774G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43067781 | |||||||
chr8:43067805 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.402-1750C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43067805 | |||||||
chr8:43067930 | T | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0091 a0001c0001t0001g0174 others(4): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.402-1625T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43067930 | |||||||
chr8:43067995 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.402-1560C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43067995 | |||||||
chr8:43068148 | G | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0072 others(12): Show |
24 | HG01243.hp1 HG01261.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.402-1407G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43068148 | |||||||
chr8:43068769 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0089 |
5 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.402-786A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43068769 | |||||||
chr8:43068878 | G | A | 32 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0071 others(29): Show |
43 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.402-677G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43068878 | |||||||
chr8:43069153 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.402-402T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43069153 | |||||||
chr8:43069243 | A | C | 1 | a0001c0001t0001g0032 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.402-312A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43069243 | |||||||
chr8:43069308 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0153 |
3 | HG01358.hp2 HG02602.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.402-247C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43069308 | |||||||
chr8:43069406 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.402-149C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 3/8 | chr8 | 43069406 | |||||||
chr8:43069835 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.506+176G>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43069835 | |||||||
chr8:43070002 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.506+343C>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43070002 | |||||||
chr8:43070120 | GGCGTGCC others(22): Show |
G | 2 | a0001c0001t0001g0024 a0001c0003t0001g0192 |
3 | HG02135.hp1 HG02723.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.506+516_506+544del others(29): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 43070120 | ||||||
chr8:43070122 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.506+463C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43070122 | |||||||
chr8:43070152 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0136 |
2 | NA18955.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.506+493G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43070152 | |||||||
chr8:43070193 | C | A | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.506+534C>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43070193 | |||||||
chr8:43070291 | G | A | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+632G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43070291 | |||||||
chr8:43070309 | AAAAAAAT | A | 8 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0068 others(5): Show |
16 | HG01243.hp1 HG02109.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.506+668_506+674del others(7): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 43070309 | ||||||
chr8:43070341 | AC | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0072 others(12): Show |
24 | HG01243.hp1 HG01261.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.506+683delC | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43070341 | |||||||
chr8:43070555 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0137 a0001c0001t0001g0147 |
5 | NA18954.hp2 NA18985.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.506+896G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43070555 | |||||||
chr8:43070562 | T | A | 1 | a0001c0003t0001g0192 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.506+903T>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43070562 | |||||||
chr8:43070970 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.507-1211A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43070970 | |||||||
chr8:43071037 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.507-1144C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43071037 | |||||||
chr8:43071675 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.507-506C>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43071675 | |||||||
chr8:43071694 | C | CA | 15 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0059 others(12): Show |
16 | HG00673.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.507-470dupA | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 43071694 | ||||||
chr8:43071694 | CA | C | 27 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0033 others(24): Show |
39 | HG00438.hp2 HG01069.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.507-470delA | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 43071694 | ||||||
chr8:43071706 | A | C | 1 | a0001c0001t0001g0017 | 2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.507-475A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43071706 | |||||||
chr8:43071978 | A | T | 1 | a0001c0003t0001g0192 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.507-203A>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43071978 | |||||||
chr8:43072044 | A | G | 15 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0072 others(12): Show |
24 | HG01243.hp1 HG01261.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.507-137A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 4/8 | chr8 | 43072044 | |||||||
chr8:43072414 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.633+107A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43072414 | |||||||
chr8:43072466 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.633+159C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43072466 | |||||||
chr8:43072721 | T | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0071 others(25): Show |
39 | HG01192.hp2 HG01243.hp1 HG01261.hp1 others(36): Show |
intron_variant | MODIFIER | c.633+414T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43072721 | |||||||
chr8:43072730 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.633+423T>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43072730 | |||||||
chr8:43072739 | A | C | 1 | a0001c0002t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.633+432A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43072739 | |||||||
chr8:43072802 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG00099.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.633+495T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43072802 | |||||||
chr8:43072878 | G | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.633+571G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43072878 | |||||||
chr8:43073215 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.633+908G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073215 | |||||||
chr8:43073301 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.633+994A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073301 | |||||||
chr8:43073340 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.633+1033G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073340 | |||||||
chr8:43073386 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.633+1079C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073386 | |||||||
chr8:43073485 | G | T | 1 | a0001c0001t0001g0147 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.633+1178G>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073485 | |||||||
chr8:43073584 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.633+1277A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073584 | |||||||
chr8:43073616 | T | A | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.633+1309T>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073616 | |||||||
chr8:43073625 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.633+1318C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073625 | |||||||
chr8:43073663 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.633+1356A>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073663 | |||||||
chr8:43073754 | G | C | 16 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0072 others(13): Show |
25 | HG01243.hp1 HG01261.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.633+1447G>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073754 | |||||||
chr8:43073932 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.633+1625A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073932 | |||||||
chr8:43073991 | C | G | 1 | a0001c0001t0001g0037 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.633+1684C>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43073991 | |||||||
chr8:43074024 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.633+1717C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43074024 | |||||||
chr8:43074025 | G | A | 5 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0068 others(2): Show |
13 | HG01243.hp1 HG02615.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.633+1718G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43074025 | |||||||
chr8:43074083 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.633+1776C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43074083 | |||||||
chr8:43074247 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.633+1940G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43074247 | |||||||
chr8:43074261 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0054 a0001c0001t0001g0059 |
4 | HG02683.hp1 HG02738.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.633+1954C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43074261 | |||||||
chr8:43074351 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0068 others(5): Show |
16 | HG01243.hp1 HG02109.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.633+2044C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43074351 | |||||||
chr8:43074352 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.633+2045G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43074352 | |||||||
chr8:43074368 | CA | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01069.hp1 HG01071.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.633+2068delA | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 43074368 | ||||||
chr8:43074374 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.633+2067A>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43074374 | |||||||
chr8:43074524 | C | CAATT | 20 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0072 others(17): Show |
29 | HG01243.hp1 HG01261.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.633+2219_633+2220i others(6): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 43074524 | ||||||
chr8:43074550 | T | TAC | 9 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0075 others(6): Show |
12 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.633+2262_633+2263d others(4): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 43074550 | ||||||
chr8:43074550 | TAC | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(119): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.633+2262_633+2263d others(4): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 43074550 | ||||||
chr8:43074568 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.633+2261C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43074568 | |||||||
chr8:43074679 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.633+2372T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43074679 | |||||||
chr8:43075030 | A | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0125 |
2 | HG01106.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.634-2186A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43075030 | |||||||
chr8:43075224 | G | A | 1 | a0001c0002t0001g0018 | 2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.634-1992G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43075224 | |||||||
chr8:43075310 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.634-1906G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43075310 | |||||||
chr8:43075357 | TCTTA | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.634-1855_634-1852d others(6): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 43075357 | ||||||
chr8:43075425 | ATTAT | A | 16 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0072 others(13): Show |
25 | HG01243.hp1 HG01261.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.634-1786_634-1783d others(6): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 43075425 | ||||||
chr8:43075598 | T | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0143 |
3 | HG00140.hp2 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.634-1618T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43075598 | |||||||
chr8:43075643 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(188): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.634-1573T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43075643 | |||||||
chr8:43075740 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.634-1476T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43075740 | |||||||
chr8:43075862 | CTTTTCT | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0054 a0001c0001t0001g0059 |
4 | HG02683.hp1 HG02738.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.634-1337_634-1332d others(8): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 43075862 | ||||||
chr8:43075879 | C | CT | 23 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0071 others(20): Show |
32 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.634-1325dupT | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 43075879 | ||||||
chr8:43075935 | C | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0123 |
2 | HG02056.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.634-1281C>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43075935 | |||||||
chr8:43076004 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.634-1212C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076004 | |||||||
chr8:43076100 | A | G | 1 | a0001c0002t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.634-1116A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076100 | |||||||
chr8:43076137 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.634-1079G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076137 | |||||||
chr8:43076244 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG02056.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.634-972A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076244 | |||||||
chr8:43076295 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.634-921C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076295 | |||||||
chr8:43076396 | C | T | 5 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0068 others(2): Show |
13 | HG01243.hp1 HG02615.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.634-820C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076396 | |||||||
chr8:43076432 | C | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02280.hp2 HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.634-784C>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076432 | |||||||
chr8:43076605 | C | T | 5 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0068 others(2): Show |
13 | HG01243.hp1 HG02615.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.634-611C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076605 | |||||||
chr8:43076745 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(146): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.634-471C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076745 | |||||||
chr8:43076774 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.634-442G>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076774 | |||||||
chr8:43076855 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.634-361C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43076855 | |||||||
chr8:43077045 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0073 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.634-171C>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43077045 | |||||||
chr8:43077209 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp2 | splice_region_variant&intron_variant | LOW | c.634-7C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 5/8 | chr8 | 43077209 | |||||||
chr8:43077500 | G | C | 32 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0071 others(29): Show |
43 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.782+136G>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43077500 | |||||||
chr8:43077591 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.782+227T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43077591 | |||||||
chr8:43077597 | T | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0049 others(5): Show |
12 | HG01070.hp2 HG01934.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.782+233T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43077597 | |||||||
chr8:43077809 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.782+445C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43077809 | |||||||
chr8:43077814 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.782+450C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43077814 | |||||||
chr8:43077976 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.782+612A>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43077976 | |||||||
chr8:43078279 | C | G | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.782+915C>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43078279 | |||||||
chr8:43078323 | T | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0072 others(16): Show |
28 | HG01243.hp1 HG01261.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.782+959T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43078323 | |||||||
chr8:43078340 | T | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(124): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.782+976T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43078340 | |||||||
chr8:43078415 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.782+1051A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43078415 | |||||||
chr8:43079046 | G | C | 1 | a0001c0002t0001g0018 | 2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.782+1682G>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43079046 | |||||||
chr8:43079173 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.782+1809C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43079173 | |||||||
chr8:43079215 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.782+1851T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43079215 | |||||||
chr8:43079243 | T | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.782+1879T>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43079243 | |||||||
chr8:43079335 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.782+1971A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43079335 | |||||||
chr8:43079340 | G | C | 1 | a0001c0001t0001g0019 | 2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.782+1976G>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43079340 | |||||||
chr8:43079439 | T | G | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.782+2075T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43079439 | |||||||
chr8:43079446 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.782+2082A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43079446 | |||||||
chr8:43079515 | CTGT | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.782+2156_782+2158d others(5): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr8 | 43079515 | ||||||
chr8:43079624 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.782+2260G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43079624 | |||||||
chr8:43079758 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.782+2394A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43079758 | |||||||
chr8:43080024 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0067 |
8 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+2660C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43080024 | |||||||
chr8:43080092 | A | T | 1 | a0001c0001t0001g0050 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.782+2728A>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43080092 | |||||||
chr8:43080219 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0111 |
3 | HG00621.hp2 NA18965.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.782+2855A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43080219 | |||||||
chr8:43080911 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.783-2207C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43080911 | |||||||
chr8:43081071 | C | T | 15 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(12): Show |
23 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.783-2047C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43081071 | |||||||
chr8:43081499 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.783-1619G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43081499 | |||||||
chr8:43081737 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.783-1381A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43081737 | |||||||
chr8:43081827 | G | T | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.783-1291G>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43081827 | |||||||
chr8:43081982 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.783-1136C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43081982 | |||||||
chr8:43082109 | G | T | 1 | a0001c0001t0001g0027 | 2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.783-1009G>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43082109 | |||||||
chr8:43082130 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0151 others(7): Show |
17 | HG00673.hp1 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.783-988A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43082130 | |||||||
chr8:43082156 | GAGCAATT others(9): Show |
G | 1 | a0001c0001t0001g0160 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.783-956_783-941del others(16): Show |
FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr8 | 43082156 | ||||||
chr8:43082169 | G | A | 1 | a0001c0003t0001g0192 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.783-949G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43082169 | |||||||
chr8:43082362 | T | A | 7 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0035 others(4): Show |
9 | HG01106.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.783-756T>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43082362 | |||||||
chr8:43082430 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.783-688G>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43082430 | |||||||
chr8:43082442 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01515.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.783-676C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43082442 | |||||||
chr8:43082465 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.783-653C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43082465 | |||||||
chr8:43082722 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.783-396T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43082722 | |||||||
chr8:43082994 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.783-124T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | chr8 | 43082994 | |||||||
chr8:43083047 | G | GA | 12 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
14 | HG00642.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.783-58dupA | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr8 | 43083047 | ||||||
chr8:43083186 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG00597.hp1 | splice_region_variant&intron_variant | LOW | c.845+6A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43083186 | |||||||
chr8:43083224 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01978.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.845+44G>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43083224 | |||||||
chr8:43083420 | A | C | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.845+240A>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43083420 | |||||||
chr8:43083562 | T | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0151 others(4): Show |
14 | HG00673.hp1 HG01358.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.845+382T>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43083562 | |||||||
chr8:43083718 | A | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0142 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.845+538A>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43083718 | |||||||
chr8:43083901 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | NA18998.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.845+721C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43083901 | |||||||
chr8:43083907 | T | C | 1 | a0001c0002t0001g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.845+727T>C | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43083907 | |||||||
chr8:43083998 | G | A | 1 | a0001c0003t0001g0192 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.846-712G>A | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43083998 | |||||||
chr8:43084050 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.846-660C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43084050 | |||||||
chr8:43084190 | A | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0051 |
3 | HG00597.hp1 NA18946.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.846-520A>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43084190 | |||||||
chr8:43084217 | C | CT | 18 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0059 others(15): Show |
18 | HG00642.hp1 HG01192.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.846-474dupT | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 43084217 | ||||||
chr8:43084217 | CT | C | 20 | a0001c0001t0001g0030 a0001c0001t0001g0071 a0001c0001t0001g0072 others(17): Show |
29 | HG00423.hp1 HG01243.hp1 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.846-474delT | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 43084217 | ||||||
chr8:43084584 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.846-126C>T | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 7/8 | chr8 | 43084584 | |||||||
chr8:43084999 | T | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0053 |
6 | HG01070.hp2 HG01934.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+118T>G | FNTA | ENSG00000168522.13 | transcript | ENST00000302279.8 | protein_coding | 8/8 | chr8 | 43084999 |