Item | Value |
---|---|
geneid | 84624 |
ensemblid | ENSG00000164694.17 |
hgncid | 21184 |
symbol | FNDC1 |
name | fibronectin type III domain containing 1 |
refseq_nuc | NM_032532.3 |
refseq_prot | NP_115921.2 |
ensembl_nuc | ENST00000297267.14 |
ensembl_prot | ENSP00000297267.9 |
mane_status | MANE Select |
chr | chr6 |
start | 159169400 |
end | 159272108 |
strand | + |
ver | v1.2 |
region | chr6:159169400-159272108 |
region5000 | chr6:159164400-159277108 |
regionname0 | FNDC1_chr6_159169400_159272108 |
regionname5000 | FNDC1_chr6_159164400_159277108 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1888 | 52 | 13 | 10 | 11 | 6 | 12 | 10 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0002 | 0/0 | 1888 | 47 | 12 | 15 | 12 | 3 | 5 | 8 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0003 | 0/0 | 1888 | 45 | 11 | 6 | 23 | 0 | 5 | 17 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0004 | 0/0 | 1888 | 40 | 10 | 2 | 21 | 2 | 5 | 19 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0005 | 0/1 | 1894 | 39 | 15 | 2 | 20 | 0 | 1 | 18 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0006 | 0/0 | 1894 | 18 | 3 | 2 | 11 | 0 | 2 | 8 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0007 | 0/0 | 1894 | 8 | 0 | 7 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0008 | 0/0 | 1894 | 8 | 3 | 0 | 2 | 0 | 3 | 2 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0009 | 0/0 | 1888 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0010 | 0/0 | 1894 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0011 | 0/0 | 1894 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0012 | 0/0 | 1888 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0013 | 0/0 | 1894 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0014 | 0/0 | 1888 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0015 | 0/0 | 1888 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0016 | 0/0 | 1888 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0017 | 0/0 | 1894 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0018 | 0/0 | 1888 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0019 | 1/0 | 1894 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0020 | 0/0 | 1888 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0021 | 0/0 | 1894 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0022 | 0/0 | 1888 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0023 | 0/0 | 1888 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0024 | 0/0 | 1894 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0025 | 0/0 | 1894 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0026 | 0/0 | 1894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0027 | 0/0 | 1894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0028 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0029 | 0/0 | 1888 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0030 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0031 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0032 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0033 | 0/0 | 1888 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0034 | 0/0 | 1888 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0035 | 0/0 | 1888 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0036 | 0/0 | 1894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
a0037 | 0/0 | 1888 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1883): Show |
chr6 | 159164400 | 159277108 |
a0038 | 0/0 | 1894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | MAPEA others(1889): Show |
chr6 | 159164400 | 159277108 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0005 | 0/0 | 5664 | 21 | 4 | 7 | 8 | 0 | 2 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0001c0006 | 0/0 | 5664 | 18 | 4 | 3 | 1 | 6 | 4 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0001c0010 | 0/0 | 5664 | 7 | 2 | 0 | 1 | 0 | 4 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0001c0033 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0001c0055 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0001c0057 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0001c0061 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0001c0062 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0001c0063 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0002c0004 | 0/0 | 5664 | 23 | 5 | 7 | 8 | 1 | 2 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0002c0008 | 0/0 | 5664 | 15 | 0 | 7 | 4 | 1 | 3 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0002c0017 | 0/0 | 5664 | 3 | 3 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0002c0018 | 0/0 | 5664 | 3 | 1 | 1 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0002c0021 | 0/0 | 5664 | 2 | 2 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0002c0039 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0003c0001 | 0/0 | 5664 | 35 | 5 | 6 | 19 | 0 | 5 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0003c0012 | 0/0 | 5664 | 4 | 4 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0003c0022 | 0/0 | 5664 | 2 | 0 | 0 | 2 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0003c0043 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0003c0045 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0003c0046 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0003c0051 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0004c0003 | 0/0 | 5664 | 29 | 3 | 2 | 17 | 2 | 5 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0004c0019 | 0/0 | 5664 | 3 | 0 | 0 | 3 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0004c0020 | 0/0 | 5664 | 3 | 3 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0004c0034 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0004c0053 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0004c0067 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0004c0068 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0004c0069 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0005c0002 | 0/1 | 5682 | 34 | 12 | 0 | 20 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0005c0015 | 0/0 | 5682 | 3 | 3 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0005c0029 | 0/0 | 5682 | 2 | 0 | 2 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0006c0007 | 0/0 | 5682 | 16 | 3 | 2 | 11 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0006c0026 | 0/0 | 5682 | 2 | 0 | 0 | 0 | 0 | 2 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0007c0009 | 0/0 | 5682 | 7 | 0 | 6 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0007c0052 | 0/0 | 5682 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0008c0011 | 0/0 | 5682 | 5 | 2 | 0 | 0 | 0 | 3 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0008c0028 | 0/0 | 5682 | 2 | 0 | 0 | 2 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0008c0070 | 0/0 | 5682 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0009c0013 | 0/0 | 5664 | 4 | 3 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0009c0032 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0010c0014 | 0/0 | 5682 | 4 | 0 | 4 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0011c0023 | 0/0 | 5682 | 2 | 2 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0011c0048 | 0/0 | 5682 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0011c0049 | 0/0 | 5682 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0012c0016 | 0/0 | 5664 | 3 | 3 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0012c0037 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0013c0024 | 0/0 | 5682 | 2 | 0 | 0 | 1 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0014c0027 | 0/0 | 5664 | 2 | 0 | 2 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0015c0030 | 0/0 | 5664 | 2 | 2 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0016c0031 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0016c0054 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0017c0025 | 0/0 | 5682 | 2 | 0 | 0 | 2 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0018c0042 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0018c0047 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0019c0066 | 1/0 | 5682 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0020c0059 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0021c0050 | 0/0 | 5682 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0022c0056 | 0/0 | 5664 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0023c0044 | 0/0 | 5664 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0024c0073 | 0/0 | 5682 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0025c0072 | 0/0 | 5682 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0026c0041 | 0/0 | 5682 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0027c0035 | 0/0 | 5682 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0028c0036 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0029c0058 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0030c0064 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0031c0040 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0032c0075 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0033c0074 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0034c0038 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0035c0060 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0036c0071 | 0/0 | 5682 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 | ||
a0037c0065 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5659): Show |
chr6 | 159164400 | 159277108 | ||
a0038c0076 | 0/0 | 5682 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | ATGGC others(5677): Show |
chr6 | 159164400 | 159277108 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0005t0001 | 0/0 | 6530 | 20 | 4 | 7 | 7 | 0 | 2 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0001c0005t0006 | 0/0 | 6530 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0001c0006t0001 | 0/0 | 6530 | 18 | 4 | 3 | 1 | 6 | 4 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0001c0010t0003 | 0/0 | 6530 | 7 | 2 | 0 | 1 | 0 | 4 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0001c0033t0001 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0001c0055t0003 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0001c0057t0002 | 0/0 | 6530 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0001c0061t0001 | 0/0 | 6530 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0001c0062t0001 | 0/0 | 6530 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0001c0063t0002 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0002c0004t0001 | 0/0 | 6530 | 22 | 5 | 6 | 8 | 1 | 2 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0002c0004t0007 | 0/0 | 6530 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0002c0008t0001 | 0/0 | 6530 | 15 | 0 | 7 | 4 | 1 | 3 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0002c0017t0002 | 0/0 | 6530 | 3 | 3 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0002c0018t0003 | 0/0 | 6530 | 2 | 0 | 1 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0002c0018t0004 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0002c0021t0001 | 0/0 | 6530 | 2 | 2 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0002c0039t0002 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0003c0001t0002 | 0/0 | 6530 | 35 | 5 | 6 | 19 | 0 | 5 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0003c0012t0004 | 0/0 | 6530 | 4 | 4 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0003c0022t0001 | 0/0 | 6530 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0003c0022t0002 | 0/0 | 6530 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0003c0043t0002 | 0/0 | 6530 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0003c0045t0001 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0003c0046t0002 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0003c0051t0002 | 0/0 | 6530 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0004c0003t0002 | 0/0 | 6530 | 29 | 3 | 2 | 17 | 2 | 5 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0004c0019t0001 | 0/0 | 6530 | 3 | 0 | 0 | 3 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0004c0020t0001 | 0/0 | 6530 | 3 | 3 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0004c0034t0004 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0004c0053t0003 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0004c0067t0003 | 0/0 | 6530 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0004c0068t0004 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0004c0069t0001 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0005c0002t0001 | 0/1 | 6548 | 34 | 12 | 0 | 20 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0005c0015t0001 | 0/0 | 6548 | 3 | 3 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0005c0029t0001 | 0/0 | 6548 | 2 | 0 | 2 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0006c0007t0001 | 0/0 | 6548 | 16 | 3 | 2 | 11 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0006c0026t0001 | 0/0 | 6548 | 2 | 0 | 0 | 0 | 0 | 2 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0007c0009t0002 | 0/0 | 6548 | 6 | 0 | 6 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0007c0009t0003 | 0/0 | 6548 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0007c0052t0003 | 0/0 | 6548 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0008c0011t0002 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0008c0011t0003 | 0/0 | 6548 | 4 | 1 | 0 | 0 | 0 | 3 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0008c0028t0002 | 0/0 | 6548 | 2 | 0 | 0 | 2 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0008c0070t0005 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0009c0013t0002 | 0/0 | 6530 | 4 | 3 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0009c0032t0003 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0010c0014t0002 | 0/0 | 6548 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0010c0014t0003 | 0/0 | 6548 | 3 | 0 | 3 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0011c0023t0002 | 0/0 | 6548 | 2 | 2 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0011c0048t0002 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0011c0049t0002 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0012c0016t0002 | 0/0 | 6530 | 3 | 3 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0012c0037t0002 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0013c0024t0001 | 0/0 | 6548 | 2 | 0 | 0 | 1 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0014c0027t0001 | 0/0 | 6530 | 2 | 0 | 2 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0015c0030t0003 | 0/0 | 6530 | 2 | 2 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0016c0031t0003 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0016c0054t0003 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0017c0025t0001 | 0/0 | 6548 | 2 | 0 | 0 | 2 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0018c0042t0002 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0018c0047t0002 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0019c0066t0003 | 1/0 | 6548 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0020c0059t0001 | 0/0 | 6530 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0021c0050t0001 | 0/0 | 6548 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0022c0056t0001 | 0/0 | 6530 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0023c0044t0001 | 0/0 | 6530 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0024c0073t0003 | 0/0 | 6548 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0025c0072t0001 | 0/0 | 6548 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0026c0041t0002 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0027c0035t0001 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0028c0036t0003 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0029c0058t0001 | 0/0 | 6530 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0030c0064t0001 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0031c0040t0002 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0032c0075t0002 | 0/0 | 6530 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0033c0074t0001 | 0/0 | 6530 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0034c0038t0002 | 0/0 | 6530 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0035c0060t0001 | 0/0 | 6530 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0036c0071t0001 | 0/0 | 6548 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
a0037c0065t0001 | 0/0 | 6530 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6525): Show |
chr6 | 159164400 | 159277108 |
a0038c0076t0001 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | AGTGG others(6543): Show |
chr6 | 159164400 | 159277108 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0005t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0010t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0010t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0010t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0010t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0010t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0010t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0010t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0033t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0055t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0057t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0061t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0062t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0001c0063t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0004t0007g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0008t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0017t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0017t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0018t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0018t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0018t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0021t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0021t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0002c0039t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0012t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0012t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0012t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0012t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0022t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0022t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0043t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0045t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0046t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0003c0051t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0019t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0019t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0019t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0020t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0020t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0020t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0034t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0053t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0067t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0068t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0004c0069t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0015t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0015t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0015t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0029t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0005c0029t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0007t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0026t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0006c0026t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0007c0009t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0007c0009t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0007c0009t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0007c0009t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0007c0009t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0007c0009t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0007c0009t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0007c0052t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0008c0011t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0008c0011t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0008c0011t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0008c0011t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0008c0011t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0008c0028t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0008c0028t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0008c0070t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0009c0013t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0009c0013t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0009c0013t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0009c0013t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0009c0032t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0010c0014t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0010c0014t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0010c0014t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0011c0023t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0011c0023t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0011c0048t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0011c0049t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0012c0016t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0012c0016t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0012c0016t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0012c0037t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0013c0024t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0013c0024t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0014c0027t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0014c0027t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0015c0030t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0015c0030t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0016c0031t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0016c0054t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0017c0025t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0017c0025t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0018c0042t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0018c0047t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0019c0066t0003g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0020c0059t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0021c0050t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0022c0056t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0023c0044t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0024c0073t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0025c0072t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0026c0041t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0027c0035t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0028c0036t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0029c0058t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0030c0064t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0031c0040t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0032c0075t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0033c0074t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0034c0038t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0035c0060t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0036c0071t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0037c0065t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
a0038c0076t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0018 | t0003 | g0220 | EUR | GBR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00140 | hp2 | a0004 | c0003 | t0002 | g0095 | EUR | GBR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00280 | hp1 | a0001 | c0006 | t0001 | g0045 | EUR | FIN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00280 | hp2 | a0004 | c0003 | t0002 | g0130 | EUR | FIN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00408 | hp1 | a0004 | c0003 | t0002 | g0109 | EAS | CHS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00408 | hp2 | a0001 | c0005 | t0001 | g0050 | EAS | CHS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00438 | hp1 | a0003 | c0051 | t0002 | g0264 | EAS | CHS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00438 | hp2 | a0002 | c0004 | t0001 | g0263 | EAS | CHS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00544 | hp1 | a0004 | c0003 | t0002 | g0114 | EAS | CHS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00544 | hp2 | a0013 | c0024 | t0001 | g0190 | EAS | CHS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00621 | hp1 | a0003 | c0001 | t0002 | g0267 | EAS | CHS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00621 | hp2 | a0020 | c0059 | t0001 | g0140 | EAS | CHS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00639 | hp1 | a0002 | c0018 | t0003 | g0219 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00639 | hp2 | a0001 | c0005 | t0001 | g0123 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00673 | hp1 | a0021 | c0050 | t0001 | g0278 | EAS | CHS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00673 | hp2 | a0003 | c0001 | t0002 | g0279 | EAS | CHS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00733 | hp1 | a0005 | c0029 | t0001 | g0056 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00733 | hp2 | a0001 | c0005 | t0001 | g0098 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00735 | hp1 | a0003 | c0001 | t0002 | g0006 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00735 | hp2 | a0005 | c0029 | t0001 | g0061 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00738 | hp1 | a0002 | c0004 | t0001 | g0193 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00738 | hp2 | a0014 | c0027 | t0001 | g0078 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00741 | hp1 | a0022 | c0056 | t0001 | g0124 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG00741 | hp2 | a0010 | c0014 | t0002 | g0076 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01069 | hp1 | a0010 | c0014 | t0003 | g0002 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01069 | hp2 | a0002 | c0004 | t0007 | g0208 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01071 | hp1 | a0010 | c0014 | t0003 | g0002 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01071 | hp2 | a0002 | c0008 | t0001 | g0206 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01074 | hp1 | a0001 | c0005 | t0001 | g0106 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01074 | hp2 | a0002 | c0008 | t0001 | g0235 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01081 | hp1 | a0014 | c0027 | t0001 | g0077 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01081 | hp2 | a0002 | c0004 | t0001 | g0221 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01109 | hp1 | a0023 | c0044 | t0001 | g0296 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01109 | hp2 | a0006 | c0007 | t0001 | g0272 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01167 | hp1 | a0003 | c0001 | t0002 | g0214 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01167 | hp2 | a0007 | c0009 | t0002 | g0274 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01169 | hp1 | a0003 | c0001 | t0002 | g0006 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01169 | hp2 | a0002 | c0004 | t0001 | g0209 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01175 | hp1 | a0002 | c0008 | t0001 | g0261 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01175 | hp2 | a0001 | c0006 | t0001 | g0111 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01192 | hp1 | a0001 | c0005 | t0001 | g0082 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01192 | hp2 | a0007 | c0009 | t0002 | g0256 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01243 | hp1 | a0001 | c0005 | t0001 | g0094 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01243 | hp2 | a0009 | c0013 | t0002 | g0029 | AMR | PUR | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01255 | hp1 | a0024 | c0073 | t0003 | g0011 | AMR | CLM | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01255 | hp2 | a0007 | c0009 | t0002 | g0257 | AMR | CLM | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01256 | hp1 | a0002 | c0004 | t0001 | g0164 | AMR | CLM | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01256 | hp2 | a0001 | c0006 | t0001 | g0146 | AMR | CLM | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01257 | hp1 | a0010 | c0014 | t0003 | g0019 | AMR | CLM | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01257 | hp2 | a0002 | c0008 | t0001 | g0230 | AMR | CLM | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01361 | hp1 | a0006 | c0007 | t0001 | g0273 | AMR | CLM | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01361 | hp2 | a0002 | c0004 | t0001 | g0275 | AMR | CLM | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01496 | hp1 | a0002 | c0004 | t0001 | g0228 | AMR | CLM | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01496 | hp2 | a0001 | c0006 | t0001 | g0147 | AMR | CLM | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01515 | hp1 | a0001 | c0006 | t0001 | g0071 | EUR | IBS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01515 | hp2 | a0007 | c0009 | t0003 | g0255 | EUR | IBS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01516 | hp1 | a0001 | c0006 | t0001 | g0141 | EUR | IBS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01516 | hp2 | a0001 | c0006 | t0001 | g0004 | EUR | IBS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01517 | hp1 | a0001 | c0006 | t0001 | g0004 | EUR | IBS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01517 | hp2 | a0001 | c0006 | t0001 | g0070 | EUR | IBS | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01891 | hp1 | a0005 | c0015 | t0001 | g0290 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01891 | hp2 | a0003 | c0012 | t0004 | g0186 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01934 | hp1 | a0003 | c0001 | t0002 | g0213 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01934 | hp2 | a0001 | c0005 | t0001 | g0142 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01975 | hp1 | a0001 | c0005 | t0001 | g0079 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01975 | hp2 | a0007 | c0009 | t0002 | g0254 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01978 | hp1 | a0002 | c0008 | t0001 | g0245 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01978 | hp2 | a0004 | c0003 | t0002 | g0017 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01981 | hp1 | a0007 | c0009 | t0002 | g0270 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01981 | hp2 | a0003 | c0001 | t0002 | g0218 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01993 | hp1 | a0007 | c0009 | t0002 | g0271 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG01993 | hp2 | a0002 | c0008 | t0001 | g0199 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02015 | hp1 | a0006 | c0007 | t0001 | g0202 | EAS | KHV | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02015 | hp2 | a0003 | c0001 | t0002 | g0227 | EAS | KHV | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02055 | hp1 | a0003 | c0001 | t0002 | g0215 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02055 | hp2 | a0002 | c0004 | t0001 | g0162 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02056 | hp1 | a0002 | c0004 | t0001 | g0242 | EAS | KHV | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02056 | hp2 | a0003 | c0001 | t0002 | g0246 | EAS | KHV | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02071 | hp1 | a0025 | c0072 | t0001 | g0046 | EAS | KHV | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02071 | hp2 | a0002 | c0004 | t0001 | g0240 | EAS | KHV | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02135 | hp1 | a0002 | c0008 | t0001 | g0283 | EAS | KHV | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02135 | hp2 | a0006 | c0007 | t0001 | g0247 | EAS | KHV | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02145 | hp1 | a0002 | c0004 | t0001 | g0176 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02145 | hp2 | a0005 | c0015 | t0001 | g0292 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02148 | hp1 | a0004 | c0003 | t0002 | g0104 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02148 | hp2 | a0002 | c0008 | t0001 | g0236 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02155 | hp1 | a0005 | c0002 | t0001 | g0066 | EAS | CDX | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02155 | hp2 | a0005 | c0002 | t0001 | g0135 | EAS | CDX | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02257 | hp1 | a0001 | c0006 | t0001 | g0126 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02257 | hp2 | a0001 | c0006 | t0001 | g0053 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02258 | hp1 | a0011 | c0048 | t0002 | g0184 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02258 | hp2 | a0015 | c0030 | t0003 | g0032 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02280 | hp1 | a0027 | c0035 | t0001 | g0293 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02280 | hp2 | a0003 | c0012 | t0004 | g0185 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02300 | hp1 | a0007 | c0052 | t0003 | g0222 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02300 | hp2 | a0003 | c0001 | t0002 | g0207 | AMR | PEL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02523 | hp1 | a0003 | c0001 | t0002 | g0226 | EAS | KHV | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02523 | hp2 | a0006 | c0007 | t0001 | g0258 | EAS | KHV | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02572 | hp1 | a0006 | c0007 | t0001 | g0174 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02572 | hp2 | a0004 | c0003 | t0002 | g0009 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02602 | hp1 | a0002 | c0008 | t0001 | g0224 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02602 | hp2 | a0003 | c0001 | t0002 | g0211 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02615 | hp1 | a0009 | c0013 | t0002 | g0026 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02615 | hp2 | a0005 | c0002 | t0001 | g0039 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02622 | hp1 | a0001 | c0055 | t0003 | g0062 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02622 | hp2 | a0001 | c0010 | t0003 | g0284 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02630 | hp1 | a0004 | c0034 | t0004 | g0294 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02630 | hp2 | a0002 | c0021 | t0001 | g0170 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02683 | hp1 | a0004 | c0003 | t0002 | g0010 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02683 | hp2 | a0001 | c0005 | t0001 | g0072 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02698 | hp1 | a0001 | c0057 | t0002 | g0024 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02698 | hp2 | a0001 | c0010 | t0003 | g0128 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02723 | hp1 | a0028 | c0036 | t0003 | g0165 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02723 | hp2 | a0006 | c0007 | t0001 | g0179 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02735 | hp1 | a0002 | c0004 | t0001 | g0239 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02735 | hp2 | a0029 | c0058 | t0001 | g0080 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02738 | hp1 | a0001 | c0010 | t0003 | g0043 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02738 | hp2 | a0001 | c0006 | t0001 | g0143 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02809 | hp1 | a0001 | c0005 | t0001 | g0287 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02809 | hp2 | a0003 | c0045 | t0001 | g0192 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02818 | hp1 | a0003 | c0001 | t0002 | g0178 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02818 | hp2 | a0008 | c0011 | t0003 | g0144 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02886 | hp1 | a0016 | c0054 | t0003 | g0037 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02886 | hp2 | a0002 | c0017 | t0002 | g0182 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02895 | hp1 | a0004 | c0020 | t0001 | g0107 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02895 | hp2 | a0003 | c0012 | t0004 | g0171 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02896 | hp1 | a0004 | c0020 | t0001 | g0099 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02896 | hp2 | a0005 | c0002 | t0001 | g0003 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02897 | hp1 | a0004 | c0020 | t0001 | g0100 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02897 | hp2 | a0005 | c0002 | t0001 | g0003 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02922 | hp1 | a0004 | c0003 | t0002 | g0012 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02922 | hp2 | a0012 | c0037 | t0002 | g0160 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02965 | hp1 | a0011 | c0049 | t0002 | g0159 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02965 | hp2 | a0006 | c0007 | t0001 | g0161 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02970 | hp1 | a0002 | c0004 | t0001 | g0210 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02970 | hp2 | a0005 | c0002 | t0001 | g0014 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02976 | hp1 | a0004 | c0068 | t0004 | g0149 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02976 | hp2 | a0009 | c0032 | t0003 | g0288 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03041 | hp1 | a0015 | c0030 | t0003 | g0033 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03041 | hp2 | a0008 | c0070 | t0005 | g0036 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03098 | hp1 | a0016 | c0031 | t0003 | g0289 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03098 | hp2 | a0011 | c0023 | t0002 | g0177 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03130 | hp1 | a0003 | c0001 | t0002 | g0188 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03130 | hp2 | a0001 | c0006 | t0001 | g0059 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03139 | hp1 | a0005 | c0002 | t0001 | g0150 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03139 | hp2 | a0011 | c0023 | t0002 | g0173 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03195 | hp1 | a0012 | c0016 | t0002 | g0166 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03195 | hp2 | a0005 | c0002 | t0001 | g0008 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03209 | hp1 | a0030 | c0064 | t0001 | g0040 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03209 | hp2 | a0031 | c0040 | t0002 | g0167 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03225 | hp1 | a0004 | c0069 | t0001 | g0007 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03225 | hp2 | a0003 | c0001 | t0002 | g0191 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03239 | hp1 | a0004 | c0003 | t0002 | g0103 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03239 | hp2 | a0008 | c0011 | t0003 | g0021 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03453 | hp1 | a0001 | c0033 | t0001 | g0295 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03453 | hp2 | a0005 | c0002 | t0001 | g0038 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03486 | hp1 | a0032 | c0075 | t0002 | g0298 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03486 | hp2 | a0008 | c0011 | t0002 | g0016 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03491 | hp1 | a0001 | c0006 | t0001 | g0148 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03491 | hp2 | a0006 | c0026 | t0001 | g0252 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03492 | hp1 | a0033 | c0074 | t0001 | g0081 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03492 | hp2 | a0006 | c0026 | t0001 | g0253 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03516 | hp1 | a0004 | c0003 | t0002 | g0068 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03516 | hp2 | a0002 | c0004 | t0001 | g0183 | AFR | ESN | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03540 | hp1 | a0001 | c0063 | t0002 | g0285 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03540 | hp2 | a0002 | c0039 | t0002 | g0205 | AFR | GWD | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03579 | hp1 | a0005 | c0002 | t0001 | g0028 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03579 | hp2 | a0002 | c0017 | t0002 | g0005 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03669 | hp1 | a0034 | c0038 | t0002 | g0152 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03669 | hp2 | a0035 | c0060 | t0001 | g0125 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03688 | hp1 | a0002 | c0008 | t0001 | g0297 | SAS | STU | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03688 | hp2 | a0004 | c0003 | t0002 | g0127 | SAS | STU | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03710 | hp1 | a0002 | c0008 | t0001 | g0229 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03710 | hp2 | a0005 | c0002 | t0001 | g0151 | SAS | PJL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03831 | hp1 | a0001 | c0061 | t0001 | g0092 | SAS | BEB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03831 | hp2 | a0004 | c0003 | t0002 | g0105 | SAS | BEB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03834 | hp1 | a0001 | c0010 | t0003 | g0074 | SAS | BEB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03834 | hp2 | a0001 | c0005 | t0001 | g0087 | SAS | BEB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03927 | hp1 | a0004 | c0003 | t0002 | g0110 | SAS | BEB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03927 | hp2 | a0001 | c0010 | t0003 | g0022 | SAS | BEB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03942 | hp1 | a0008 | c0011 | t0003 | g0052 | SAS | BEB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03942 | hp2 | a0003 | c0001 | t0002 | g0265 | SAS | BEB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG04184 | hp1 | a0008 | c0011 | t0003 | g0057 | SAS | BEB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG04184 | hp2 | a0013 | c0024 | t0001 | g0234 | SAS | BEB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG04199 | hp1 | a0003 | c0001 | t0002 | g0232 | SAS | STU | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG04199 | hp2 | a0001 | c0006 | t0001 | g0020 | SAS | STU | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG04204 | hp1 | a0003 | c0001 | t0002 | g0250 | SAS | STU | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG04204 | hp2 | a0002 | c0004 | t0001 | g0212 | SAS | STU | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG04228 | hp1 | a0003 | c0001 | t0002 | g0203 | SAS | STU | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG04228 | hp2 | a0001 | c0006 | t0001 | g0084 | SAS | STU | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18522 | hp1 | a0003 | c0046 | t0002 | g0243 | AFR | YRI | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18522 | hp2 | a0005 | c0002 | t0001 | g0145 | AFR | YRI | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18906 | hp1 | a0009 | c0013 | t0002 | g0025 | AFR | YRI | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18906 | hp2 | a0005 | c0002 | t0001 | g0030 | AFR | YRI | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18947 | hp1 | a0005 | c0002 | t0001 | g0136 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18947 | hp2 | a0005 | c0002 | t0001 | g0058 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18948 | hp1 | a0006 | c0007 | t0001 | g0158 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18948 | hp2 | a0004 | c0019 | t0001 | g0096 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18953 | hp1 | a0008 | c0028 | t0002 | g0055 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18953 | hp2 | a0004 | c0003 | t0002 | g0113 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18954 | hp1 | a0005 | c0002 | t0001 | g0133 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18954 | hp2 | a0006 | c0007 | t0001 | g0251 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18956 | hp1 | a0005 | c0002 | t0001 | g0089 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18956 | hp2 | a0002 | c0004 | t0001 | g0189 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18957 | hp1 | a0003 | c0043 | t0002 | g0197 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18957 | hp2 | a0005 | c0002 | t0001 | g0064 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18960 | hp1 | a0006 | c0007 | t0001 | g0157 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18960 | hp2 | a0004 | c0003 | t0002 | g0001 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18965 | hp1 | a0005 | c0002 | t0001 | g0132 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18965 | hp2 | a0003 | c0022 | t0002 | g0217 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18968 | hp1 | a0006 | c0007 | t0001 | g0259 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18968 | hp2 | a0001 | c0005 | t0001 | g0048 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18969 | hp1 | a0005 | c0002 | t0001 | g0134 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18969 | hp2 | a0003 | c0001 | t0002 | g0277 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18970 | hp1 | a0003 | c0001 | t0002 | g0198 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18970 | hp2 | a0001 | c0005 | t0001 | g0047 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18974 | hp1 | a0004 | c0003 | t0002 | g0102 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18974 | hp2 | a0003 | c0001 | t0002 | g0281 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18980 | hp1 | a0001 | c0006 | t0001 | g0088 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18980 | hp2 | a0003 | c0001 | t0002 | g0262 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18982 | hp1 | a0002 | c0004 | t0001 | g0241 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18982 | hp2 | a0003 | c0001 | t0002 | g0260 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18983 | hp1 | a0002 | c0004 | t0001 | g0196 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18983 | hp2 | a0003 | c0001 | t0002 | g0266 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18987 | hp1 | a0004 | c0003 | t0002 | g0129 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18987 | hp2 | a0005 | c0002 | t0001 | g0122 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18989 | hp1 | a0005 | c0002 | t0001 | g0067 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18989 | hp2 | a0003 | c0001 | t0002 | g0216 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18992 | hp1 | a0003 | c0001 | t0002 | g0156 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18992 | hp2 | a0017 | c0025 | t0001 | g0237 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18993 | hp1 | a0004 | c0003 | t0002 | g0085 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18993 | hp2 | a0017 | c0025 | t0001 | g0200 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18994 | hp1 | a0004 | c0003 | t0002 | g0115 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18994 | hp2 | a0002 | c0008 | t0001 | g0195 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19000 | hp1 | a0036 | c0071 | t0001 | g0035 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19000 | hp2 | a0003 | c0001 | t0002 | g0268 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19003 | hp1 | a0003 | c0001 | t0002 | g0233 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19003 | hp2 | a0005 | c0002 | t0001 | g0121 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19007 | hp1 | a0003 | c0001 | t0002 | g0276 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19007 | hp2 | a0005 | c0002 | t0001 | g0119 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19011 | hp1 | a0001 | c0062 | t0001 | g0083 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19011 | hp2 | a0004 | c0003 | t0002 | g0042 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19012 | hp1 | a0004 | c0003 | t0002 | g0097 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19012 | hp2 | a0001 | c0005 | t0001 | g0073 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19030 | hp1 | a0012 | c0016 | t0002 | g0168 | AFR | LWK | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19030 | hp2 | a0005 | c0002 | t0001 | g0027 | AFR | LWK | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19043 | hp1 | a0018 | c0047 | t0002 | g0163 | AFR | LWK | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19043 | hp2 | a0003 | c0001 | t0002 | g0180 | AFR | LWK | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19056 | hp1 | a0004 | c0067 | t0003 | g0131 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19056 | hp2 | a0006 | c0007 | t0001 | g0201 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19057 | hp1 | a0004 | c0003 | t0002 | g0041 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19057 | hp2 | a0005 | c0002 | t0001 | g0069 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19062 | hp1 | a0001 | c0005 | t0001 | g0051 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19062 | hp2 | a0005 | c0002 | t0001 | g0091 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19063 | hp1 | a0004 | c0003 | t0002 | g0101 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19063 | hp2 | a0002 | c0004 | t0001 | g0154 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19064 | hp1 | a0037 | c0065 | t0001 | g0086 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19064 | hp2 | a0005 | c0002 | t0001 | g0138 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19065 | hp1 | a0004 | c0003 | t0002 | g0001 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19065 | hp2 | a0005 | c0002 | t0001 | g0065 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19066 | hp1 | a0001 | c0010 | t0003 | g0013 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19066 | hp2 | a0003 | c0001 | t0002 | g0280 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19068 | hp1 | a0005 | c0002 | t0001 | g0060 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19068 | hp2 | a0004 | c0019 | t0001 | g0063 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19070 | hp1 | a0004 | c0003 | t0002 | g0001 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19070 | hp2 | a0006 | c0007 | t0001 | g0223 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19072 | hp1 | a0006 | c0007 | t0001 | g0153 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19072 | hp2 | a0004 | c0003 | t0002 | g0112 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19076 | hp1 | a0002 | c0008 | t0001 | g0231 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19076 | hp2 | a0004 | c0003 | t0002 | g0108 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19079 | hp1 | a0005 | c0002 | t0001 | g0054 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19079 | hp2 | a0001 | c0005 | t0001 | g0139 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19080 | hp1 | a0002 | c0008 | t0001 | g0244 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19080 | hp2 | a0004 | c0003 | t0002 | g0117 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19083 | hp1 | a0003 | c0001 | t0002 | g0269 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19083 | hp2 | a0004 | c0019 | t0001 | g0116 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19084 | hp1 | a0008 | c0028 | t0002 | g0118 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19084 | hp2 | a0001 | c0005 | t0001 | g0090 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19088 | hp1 | a0003 | c0022 | t0001 | g0248 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19088 | hp2 | a0005 | c0002 | t0001 | g0120 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19091 | hp1 | a0006 | c0007 | t0001 | g0194 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19091 | hp2 | a0001 | c0005 | t0006 | g0137 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19240 | hp1 | a0001 | c0010 | t0003 | g0286 | AFR | YRI | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA19240 | hp2 | a0004 | c0053 | t0003 | g0034 | AFR | YRI | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA20129 | hp1 | a0001 | c0005 | t0001 | g0093 | AFR | ASW | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA20129 | hp2 | a0018 | c0042 | t0002 | g0282 | AFR | ASW | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA20805 | hp1 | a0002 | c0004 | t0001 | g0225 | EUR | TSI | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA20805 | hp2 | a0002 | c0008 | t0001 | g0204 | EUR | TSI | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02109 | hp1 | a0005 | c0015 | t0001 | g0291 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02109 | hp2 | a0026 | c0041 | t0002 | g0155 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02486 | hp1 | a0003 | c0012 | t0004 | g0187 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02486 | hp2 | a0005 | c0002 | t0001 | g0044 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02559 | hp1 | a0001 | c0005 | t0001 | g0015 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG02559 | hp2 | a0002 | c0017 | t0002 | g0005 | AFR | ACB | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03471 | hp1 | a0002 | c0018 | t0004 | g0175 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG03471 | hp2 | a0002 | c0021 | t0001 | g0169 | AFR | MSL | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG06807 | hp1 | a0002 | c0004 | t0001 | g0172 | AFR | USA | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
HG06807 | hp2 | a0012 | c0016 | t0002 | g0181 | AFR | USA | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18955 | hp1 | a0002 | c0004 | t0001 | g0238 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA18955 | hp2 | a0003 | c0001 | t0002 | g0249 | EAS | JPT | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA20300 | hp1 | a0001 | c0006 | t0001 | g0018 | AFR | USA | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA20300 | hp2 | a0009 | c0013 | t0002 | g0031 | AFR | USA | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA21309 | hp1 | a0001 | c0005 | t0001 | g0075 | AFR | LWK | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
NA21309 | hp2 | a0038 | c0076 | t0001 | g0299 | AFR | LWK | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
homoSapiens | chm13v2 | a0005 | c0002 | t0001 | g0049 | REF | REF | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
homoSapiens | grch38p0 | a0019 | c0066 | t0003 | g0023 | REF | REF | FNDC1_chr6_159164400_159277108 | FNDC1 | chr6 | 159164400 | 159277108 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:159169697 | C | G | 2 | a0032 a0038 |
2 | HG03486.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.101C>G | p.Ala34Gly | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/23 | 298/6548 | 101/5685 | 34/1894 | chr6 | 159169697 | |||
chr6:159169702 | T | C | 17 | a0002 a0003 a0006 others(14): Show |
140 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(137): Show |
missense_variant | MODERATE | c.106T>C | p.Ser36Pro | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/23 | 303/6548 | 106/5685 | 36/1894 | chr6 | 159169702 | |||
chr6:159199996 | A | G | 1 | a0033 | 1 | HG03492.hp1 | missense_variant&splice_region_variant | MODERATE | c.305A>G | p.Glu102Gly | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 3/23 | 502/6548 | 305/5685 | 102/1894 | chr6 | 159199996 | |||
chr6:159200055 | C | T | 3 | a0007 a0010 a0024 |
13 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
missense_variant | MODERATE | c.364C>T | p.Pro122Ser | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 3/23 | 561/6548 | 364/5685 | 122/1894 | chr6 | 159200055 | |||
chr6:159223618 | A | T | 1 | a0015 | 2 | HG02258.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.857A>T | p.Glu286Val | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/23 | 1054/6548 | 857/5685 | 286/1894 | chr6 | 159223618 | |||
chr6:159225592 | G | T | 1 | a0017 | 2 | NA18992.hp2 NA18993.hp2 |
missense_variant | MODERATE | c.942G>T | p.Gln314His | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 8/23 | 1139/6548 | 942/5685 | 314/1894 | chr6 | 159225592 | |||
chr6:159229946 | A | G | 25 | a0003 a0004 a0005 others(22): Show |
194 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(191): Show |
missense_variant | MODERATE | c.1312A>G | p.Thr438Ala | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/23 | 1509/6548 | 1312/5685 | 438/1894 | chr6 | 159229946 | |||
chr6:159231884 | A | G | 1 | a0024 | 1 | HG01255.hp1 | missense_variant&splice_region_variant | MODERATE | c.1372A>G | p.Ser458Gly | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 1569/6548 | 1372/5685 | 458/1894 | chr6 | 159231884 | |||
chr6:159231899 | G | C | 23 | a0001 a0002 a0003 others(20): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
missense_variant | MODERATE | c.1387G>C | p.Glu463Gln | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 1584/6548 | 1387/5685 | 463/1894 | chr6 | 159231899 | |||
chr6:159232383 | C | T | 1 | a0021 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.1871C>T | p.Ala624Val | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 2068/6548 | 1871/5685 | 624/1894 | chr6 | 159232383 | |||
chr6:159232435 | C | A | 1 | a0015 | 2 | HG02258.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.1923C>A | p.Asp641Glu | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 2120/6548 | 1923/5685 | 641/1894 | chr6 | 159232435 | |||
chr6:159232512 | G | A | 1 | a0022 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.2000G>A | p.Arg667Gln | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 2197/6548 | 2000/5685 | 667/1894 | chr6 | 159232512 | |||
chr6:159232889 | G | A | 2 | a0029 a0034 |
2 | HG02735.hp2 HG03669.hp1 |
missense_variant | MODERATE | c.2377G>A | p.Asp793Asn | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 2574/6548 | 2377/5685 | 793/1894 | chr6 | 159232889 | |||
chr6:159232998 | G | A | 1 | a0014 | 2 | HG00738.hp2 HG01081.hp1 |
missense_variant | MODERATE | c.2486G>A | p.Gly829Glu | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 2683/6548 | 2486/5685 | 829/1894 | chr6 | 159232998 | |||
chr6:159233376 | G | A | 4 | a0009 a0012 a0016 others(1): Show |
12 | HG01243.hp2 HG02615.hp1 HG02723.hp1 others(9): Show |
missense_variant | MODERATE | c.2864G>A | p.Ser955Asn | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3061/6548 | 2864/5685 | 955/1894 | chr6 | 159233376 | |||
chr6:159233519 | C | G | 22 | a0001 a0002 a0003 others(19): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
missense_variant | MODERATE | c.3007C>G | p.Gln1003Glu | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3204/6548 | 3007/5685 | 1003/1894 | chr6 | 159233519 | |||
chr6:159233688 | G | C | 2 | a0016 a0028 |
3 | HG02723.hp1 HG02886.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.3176G>C | p.Ser1059Thr | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3373/6548 | 3176/5685 | 1059/1894 | chr6 | 159233688 | |||
chr6:159233861 | A | G | 1 | a0037 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.3349A>G | p.Thr1117Ala | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3546/6548 | 3349/5685 | 1117/1894 | chr6 | 159233861 | |||
chr6:159233937 | G | A | 1 | a0020 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.3425G>A | p.Gly1142Asp | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3622/6548 | 3425/5685 | 1142/1894 | chr6 | 159233937 | |||
chr6:159234052 | C | G | 22 | a0001 a0002 a0003 others(19): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
missense_variant | MODERATE | c.3540C>G | p.Asp1180Glu | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3737/6548 | 3540/5685 | 1180/1894 | chr6 | 159234052 | |||
chr6:159234158 | G | A | 2 | a0018 a0032 |
3 | HG03486.hp1 NA19043.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.3646G>A | p.Asp1216Asn | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3843/6548 | 3646/5685 | 1216/1894 | chr6 | 159234158 | |||
chr6:159234216 | G | A | 1 | a0023 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.3704G>A | p.Gly1235Glu | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3901/6548 | 3704/5685 | 1235/1894 | chr6 | 159234216 | |||
chr6:159234249 | C | G | 1 | a0031 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.3737C>G | p.Pro1246Arg | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3934/6548 | 3737/5685 | 1246/1894 | chr6 | 159234249 | |||
chr6:159234294 | T | C | 22 | a0001 a0002 a0003 others(19): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
missense_variant | MODERATE | c.3782T>C | p.Leu1261Pro | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3979/6548 | 3782/5685 | 1261/1894 | chr6 | 159234294 | |||
chr6:159234321 | G | A | 1 | a0035 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3809G>A | p.Ser1270Asn | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 4006/6548 | 3809/5685 | 1270/1894 | chr6 | 159234321 | |||
chr6:159234333 | G | T | 1 | a0030 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.3821G>T | p.Gly1274Val | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 4018/6548 | 3821/5685 | 1274/1894 | chr6 | 159234333 | |||
chr6:159234351 | A | G | 22 | a0001 a0002 a0003 others(19): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
missense_variant | MODERATE | c.3839A>G | p.Gln1280Arg | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 4036/6548 | 3839/5685 | 1280/1894 | chr6 | 159234351 | |||
chr6:159239747 | GCCACCAC others(11): Show |
G | 22 | a0001 a0002 a0003 others(19): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
disruptive_inframe_deletion | MODERATE | c.4436_4453delCCCGCC others(12): Show |
p.Thr1479_Thr1484del | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/23 | 4633/6548 | 4436/5685 | 1479/1894 | INFO_REALIGN_3_PRIME | chr6 | 159239747 | ||
chr6:159239792 | C | T | 2 | a0013 a0025 |
3 | HG00544.hp2 HG02071.hp1 HG04184.hp2 |
missense_variant | MODERATE | c.4456C>T | p.Arg1486Cys | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/23 | 4653/6548 | 4456/5685 | 1486/1894 | chr6 | 159239792 | |||
chr6:159239793 | G | A | 1 | a0035 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.4457G>A | p.Arg1486His | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/23 | 4654/6548 | 4457/5685 | 1486/1894 | chr6 | 159239793 | |||
chr6:159239847 | C | A | 22 | a0001 a0002 a0003 others(19): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
missense_variant | MODERATE | c.4511C>A | p.Thr1504Lys | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/23 | 4708/6548 | 4511/5685 | 1504/1894 | chr6 | 159239847 | |||
chr6:159239919 | T | A | 2 | a0001 a0002 |
3 | HG02630.hp2 HG03453.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.4583T>A | p.Met1528Lys | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/23 | 4780/6548 | 4583/5685 | 1528/1894 | chr6 | 159239919 | |||
chr6:159249068 | A | G | 9 | a0005 a0006 a0013 others(6): Show |
65 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(62): Show |
missense_variant | MODERATE | c.4720A>G | p.Thr1574Ala | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/23 | 4917/6548 | 4720/5685 | 1574/1894 | chr6 | 159249068 | |||
chr6:159251314 | C | T | 1 | a0027 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.4847C>T | p.Thr1616Met | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/23 | 5044/6548 | 4847/5685 | 1616/1894 | chr6 | 159251314 | |||
chr6:159261225 | G | A | 1 | a0036 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.5210G>A | p.Gly1737Asp | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/23 | 5407/6548 | 5210/5685 | 1737/1894 | chr6 | 159261225 | |||
chr6:159266219 | A | C | 1 | a0002 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.5420A>C | p.Lys1807Thr | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/23 | 5617/6548 | 5420/5685 | 1807/1894 | chr6 | 159266219 | |||
chr6:159267816 | G | A | 2 | a0001 a0003 |
2 | HG03540.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.5459G>A | p.Ser1820Asn | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/23 | 5656/6548 | 5459/5685 | 1820/1894 | chr6 | 159267816 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:159169605 | C | A | 6 | a0001c0033 a0004c0034 a0005c0015 others(3): Show |
8 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
synonymous_variant | LOW | c.9C>A | p.Pro3Pro | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/23 | 206/6548 | 9/5685 | 3/1894 | chr6 | 159169605 | |||
chr6:159223640 | A | C | 1 | a0003c0051 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.879A>C | p.Ala293Ala | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/23 | 1076/6548 | 879/5685 | 293/1894 | chr6 | 159223640 | |||
chr6:159225544 | C | T | 1 | a0006c0026 | 2 | HG03491.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.894C>T | p.Thr298Thr | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 8/23 | 1091/6548 | 894/5685 | 298/1894 | chr6 | 159225544 | |||
chr6:159225577 | G | A | 1 | a0004c0053 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.927G>A | p.Arg309Arg | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 8/23 | 1124/6548 | 927/5685 | 309/1894 | chr6 | 159225577 | |||
chr6:159226552 | G | A | 7 | a0009c0013 a0009c0032 a0012c0016 others(4): Show |
12 | HG01243.hp2 HG02615.hp1 HG02723.hp1 others(9): Show |
synonymous_variant | LOW | c.1152G>A | p.Ala384Ala | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/23 | 1349/6548 | 1152/5685 | 384/1894 | chr6 | 159226552 | |||
chr6:159229816 | A | G | 1 | a0012c0016 | 3 | HG03195.hp1 HG06807.hp2 NA19030.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1182A>G | p.Glu394Glu | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/23 | 1379/6548 | 1182/5685 | 394/1894 | chr6 | 159229816 | |||
chr6:159229942 | G | A | 1 | a0001c0055 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1308G>A | p.Arg436Arg | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/23 | 1505/6548 | 1308/5685 | 436/1894 | chr6 | 159229942 | |||
chr6:159232090 | C | T | 1 | a0007c0052 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.1578C>T | p.Arg526Arg | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 1775/6548 | 1578/5685 | 526/1894 | chr6 | 159232090 | |||
chr6:159232603 | C | G | 26 | a0001c0005 a0001c0006 a0001c0010 others(23): Show |
112 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
synonymous_variant | LOW | c.2091C>G | p.Ala697Ala | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 2288/6548 | 2091/5685 | 697/1894 | chr6 | 159232603 | |||
chr6:159233455 | G | T | 53 | a0001c0005 a0001c0006 a0001c0010 others(50): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
synonymous_variant | LOW | c.2943G>T | p.Pro981Pro | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3140/6548 | 2943/5685 | 981/1894 | chr6 | 159233455 | |||
chr6:159233797 | G | A | 12 | a0001c0057 a0003c0001 a0003c0022 others(9): Show |
77 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
synonymous_variant | LOW | c.3285G>A | p.Ala1095Ala | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3482/6548 | 3285/5685 | 1095/1894 | chr6 | 159233797 | |||
chr6:159233881 | C | T | 12 | a0001c0057 a0003c0001 a0003c0022 others(9): Show |
77 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
synonymous_variant | LOW | c.3369C>T | p.Gly1123Gly | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3566/6548 | 3369/5685 | 1123/1894 | chr6 | 159233881 | |||
chr6:159233962 | A | C | 52 | a0001c0005 a0001c0006 a0001c0010 others(49): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
synonymous_variant | LOW | c.3450A>C | p.Val1150Val | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3647/6548 | 3450/5685 | 1150/1894 | chr6 | 159233962 | |||
chr6:159234070 | A | G | 52 | a0001c0005 a0001c0006 a0001c0010 others(49): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
synonymous_variant | LOW | c.3558A>G | p.Gly1186Gly | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3755/6548 | 3558/5685 | 1186/1894 | chr6 | 159234070 | |||
chr6:159234103 | T | C | 3 | a0003c0045 a0004c0020 a0023c0044 |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
synonymous_variant | LOW | c.3591T>C | p.Ser1197Ser | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 3788/6548 | 3591/5685 | 1197/1894 | chr6 | 159234103 | |||
chr6:159234370 | A | G | 52 | a0001c0005 a0001c0006 a0001c0010 others(49): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
synonymous_variant | LOW | c.3858A>G | p.Pro1286Pro | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 4055/6548 | 3858/5685 | 1286/1894 | chr6 | 159234370 | |||
chr6:159234373 | T | C | 1 | a0001c0061 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.3861T>C | p.Pro1287Pro | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/23 | 4058/6548 | 3861/5685 | 1287/1894 | chr6 | 159234373 | |||
chr6:159238631 | G | T | 1 | a0003c0043 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.4146G>T | p.Arg1382Arg | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/23 | 4343/6548 | 4146/5685 | 1382/1894 | chr6 | 159238631 | |||
chr6:159239548 | C | T | 1 | a0011c0049 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.4212C>T | p.Asp1404Asp | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/23 | 4409/6548 | 4212/5685 | 1404/1894 | chr6 | 159239548 | |||
chr6:159239821 | G | A | 1 | a0001c0062 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.4485G>A | p.Thr1495Thr | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/23 | 4682/6548 | 4485/5685 | 1495/1894 | chr6 | 159239821 | |||
chr6:159246929 | T | G | 5 | a0001c0006 a0002c0008 a0030c0064 others(2): Show |
36 | HG00280.hp1 HG01071.hp2 HG01074.hp2 others(33): Show |
synonymous_variant | LOW | c.4650T>G | p.Thr1550Thr | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/23 | 4847/6548 | 4650/5685 | 1550/1894 | chr6 | 159246929 | |||
chr6:159249043 | T | C | 1 | a0012c0037 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.4695T>C | p.Tyr1565Tyr | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/23 | 4892/6548 | 4695/5685 | 1565/1894 | chr6 | 159249043 | |||
chr6:159251387 | G | C | 14 | a0001c0057 a0002c0017 a0003c0001 others(11): Show |
81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
synonymous_variant | LOW | c.4920G>C | p.Leu1640Leu | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/23 | 5117/6548 | 4920/5685 | 1640/1894 | chr6 | 159251387 | |||
chr6:159251423 | C | T | 22 | a0001c0005 a0001c0006 a0001c0033 others(19): Show |
102 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
synonymous_variant | LOW | c.4956C>T | p.Asp1652Asp | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/23 | 5153/6548 | 4956/5685 | 1652/1894 | chr6 | 159251423 | |||
chr6:159251510 | C | T | 14 | a0001c0057 a0002c0017 a0003c0001 others(11): Show |
81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
synonymous_variant | LOW | c.5043C>T | p.Ala1681Ala | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/23 | 5240/6548 | 5043/5685 | 1681/1894 | chr6 | 159251510 | |||
chr6:159271373 | C | T | 12 | a0005c0002 a0005c0015 a0006c0007 others(9): Show |
64 | HG00544.hp2 HG00673.hp1 HG01109.hp2 others(61): Show |
synonymous_variant | LOW | c.5616C>T | p.Ile1872Ile | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 23/23 | 5813/6548 | 5616/5685 | 1872/1894 | chr6 | 159271373 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:159169496 | G | A | 1 | a0008c0070t0005 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/23 | 101 | chr6 | 159169496 | ||||||
chr6:159169560 | C | A | 1 | a0001c0005t0006 | 1 | NA19091.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/23 | 37 | chr6 | 159169560 | ||||||
chr6:159271444 | C | T | 4 | a0002c0018t0004 a0003c0012t0004 a0004c0034t0004 others(1): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 23/23 | 2 | chr6 | 159271444 | ||||||
chr6:159271527 | G | A | 37 | a0001c0005t0001 a0001c0005t0006 a0001c0006t0001 others(34): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*85G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 23/23 | 85 | chr6 | 159271527 | ||||||
chr6:159271564 | T | C | 67 | a0001c0005t0001 a0001c0005t0006 a0001c0006t0001 others(64): Show |
276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*122T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 23/23 | 122 | chr6 | 159271564 | ||||||
chr6:159271762 | C | T | 1 | a0002c0004t0007 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*320C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 23/23 | 320 | chr6 | 159271762 | ||||||
chr6:159271763 | G | A | 4 | a0002c0018t0004 a0003c0012t0004 a0004c0034t0004 others(1): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*321G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 23/23 | 321 | chr6 | 159271763 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:159169747 | G | A | 3 | a0004c0003t0002g0009 a0004c0069t0001g0007 a0005c0002t0001g0008 |
3 | HG02572.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.109+42G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159169747 | |||||||
chr6:159169769 | C | T | 2 | a0032c0075t0002g0298 a0038c0076t0001g0299 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.109+64C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159169769 | |||||||
chr6:159169830 | C | T | 1 | a0002c0008t0001g0297 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.109+125C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159169830 | |||||||
chr6:159169854 | T | C | 1 | a0004c0003t0002g0010 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.109+149T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159169854 | |||||||
chr6:159169933 | T | C | 2 | a0032c0075t0002g0298 a0038c0076t0001g0299 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.109+228T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159169933 | |||||||
chr6:159169981 | A | G | 1 | a0023c0044t0001g0296 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.109+276A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159169981 | |||||||
chr6:159170010 | A | G | 2 | a0032c0075t0002g0298 a0038c0076t0001g0299 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.109+305A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159170010 | |||||||
chr6:159170025 | A | G | 2 | a0032c0075t0002g0298 a0038c0076t0001g0299 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.109+320A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159170025 | |||||||
chr6:159170103 | G | C | 2 | a0032c0075t0002g0298 a0038c0076t0001g0299 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.109+398G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159170103 | |||||||
chr6:159170178 | A | G | 12 | a0001c0005t0001g0287 a0001c0010t0003g0284 a0001c0010t0003g0286 others(9): Show |
12 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+473A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159170178 | |||||||
chr6:159170192 | C | T | 1 | a0004c0003t0002g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.109+487C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159170192 | |||||||
chr6:159170229 | A | C | 138 | a0002c0004t0001g0154 a0002c0004t0001g0162 a0002c0004t0001g0164 others(135): Show |
140 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.109+524A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159170229 | |||||||
chr6:159170397 | T | C | 1 | a0034c0038t0002g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.109+692T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159170397 | |||||||
chr6:159170526 | A | C | 278 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(275): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.109+821A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159170526 | |||||||
chr6:159170728 | G | A | 4 | a0005c0002t0001g0030 a0009c0013t0002g0029 a0009c0013t0002g0031 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+1023G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159170728 | |||||||
chr6:159171134 | C | T | 1 | a0023c0044t0001g0296 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.109+1429C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159171134 | |||||||
chr6:159171135 | C | A | 1 | a0006c0007t0001g0153 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.109+1430C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159171135 | |||||||
chr6:159171146 | C | A | 1 | a0032c0075t0002g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.109+1441C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159171146 | |||||||
chr6:159171148 | C | T | 1 | a0005c0002t0001g0151 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.109+1443C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159171148 | |||||||
chr6:159171750 | A | T | 8 | a0001c0033t0001g0295 a0004c0034t0004g0294 a0005c0015t0001g0290 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+2045A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159171750 | |||||||
chr6:159171751 | T | A | 8 | a0001c0033t0001g0295 a0004c0034t0004g0294 a0005c0015t0001g0290 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+2046T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159171751 | |||||||
chr6:159171794 | C | T | 1 | a0002c0008t0001g0283 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.109+2089C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159171794 | |||||||
chr6:159171898 | A | G | 2 | a0001c0005t0001g0287 a0001c0010t0003g0286 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.109+2193A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159171898 | |||||||
chr6:159171996 | T | C | 1 | a0023c0044t0001g0296 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.109+2291T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159171996 | |||||||
chr6:159172113 | T | C | 2 | a0004c0053t0003g0034 a0015c0030t0003g0033 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.109+2408T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159172113 | |||||||
chr6:159172274 | T | A | 1 | a0024c0073t0003g0011 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.109+2569T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159172274 | |||||||
chr6:159172324 | G | C | 1 | a0036c0071t0001g0035 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.109+2619G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159172324 | |||||||
chr6:159172770 | G | T | 2 | a0032c0075t0002g0298 a0038c0076t0001g0299 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.109+3065G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159172770 | |||||||
chr6:159172816 | A | C | 5 | a0004c0003t0002g0009 a0004c0069t0001g0007 a0005c0002t0001g0008 others(2): Show |
5 | HG02572.hp2 HG03195.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+3111A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159172816 | |||||||
chr6:159172860 | A | G | 2 | a0004c0068t0004g0149 a0005c0002t0001g0150 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.109+3155A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159172860 | |||||||
chr6:159172952 | C | T | 6 | a0001c0006t0001g0146 a0001c0006t0001g0147 a0001c0006t0001g0148 others(3): Show |
6 | HG01256.hp2 HG01496.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+3247C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159172952 | |||||||
chr6:159173067 | G | A | 17 | a0001c0005t0001g0287 a0001c0010t0003g0284 a0001c0010t0003g0286 others(14): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.109+3362G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159173067 | |||||||
chr6:159173120 | C | T | 7 | a0005c0002t0001g0003 a0005c0002t0001g0027 a0005c0002t0001g0028 others(4): Show |
8 | HG02615.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+3415C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159173120 | |||||||
chr6:159173136 | G | A | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.109+3431G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159173136 | |||||||
chr6:159173201 | G | C | 1 | a0003c0001t0002g0156 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.109+3496G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159173201 | |||||||
chr6:159173257 | T | C | 134 | a0002c0004t0001g0154 a0002c0004t0001g0162 a0002c0004t0001g0164 others(131): Show |
136 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.109+3552T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159173257 | |||||||
chr6:159173264 | G | C | 2 | a0006c0007t0001g0157 a0006c0007t0001g0158 |
2 | NA18948.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.109+3559G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159173264 | |||||||
chr6:159173279 | CCG | C | 134 | a0002c0004t0001g0154 a0002c0004t0001g0162 a0002c0004t0001g0164 others(131): Show |
136 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.109+3578_109+3579d others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159173279 | ||||||
chr6:159173375 | G | A | 1 | a0011c0049t0002g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.109+3670G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159173375 | |||||||
chr6:159173444 | A | T | 1 | a0004c0003t0002g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.109+3739A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159173444 | |||||||
chr6:159173935 | G | A | 1 | a0008c0070t0005g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.109+4230G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159173935 | |||||||
chr6:159174149 | C | T | 1 | a0001c0006t0001g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.109+4444C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174149 | |||||||
chr6:159174346 | C | T | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.109+4641C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174346 | |||||||
chr6:159174412 | C | A | 1 | a0008c0070t0005g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.109+4707C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174412 | |||||||
chr6:159174419 | G | C | 4 | a0005c0002t0001g0030 a0009c0013t0002g0029 a0009c0013t0002g0031 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+4714G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174419 | |||||||
chr6:159174492 | C | T | 2 | a0032c0075t0002g0298 a0038c0076t0001g0299 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.109+4787C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174492 | |||||||
chr6:159174527 | G | C | 38 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(35): Show |
39 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.109+4822G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174527 | |||||||
chr6:159174709 | T | G | 2 | a0004c0003t0002g0012 a0004c0003t0002g0068 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.109+5004T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174709 | |||||||
chr6:159174853 | A | G | 1 | a0001c0057t0002g0024 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.109+5148A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174853 | |||||||
chr6:159174905 | T | C | 27 | a0002c0004t0001g0164 a0002c0004t0001g0172 a0002c0004t0001g0176 others(24): Show |
28 | HG01109.hp1 HG01256.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.109+5200T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174905 | |||||||
chr6:159174916 | A | G | 2 | a0003c0001t0002g0280 a0003c0001t0002g0281 |
2 | NA18974.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.109+5211A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174916 | |||||||
chr6:159174943 | A | T | 27 | a0002c0004t0001g0164 a0002c0004t0001g0172 a0002c0004t0001g0176 others(24): Show |
28 | HG01109.hp1 HG01256.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.109+5238A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159174943 | |||||||
chr6:159175454 | T | C | 27 | a0002c0004t0001g0164 a0002c0004t0001g0172 a0002c0004t0001g0176 others(24): Show |
28 | HG01109.hp1 HG01256.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.109+5749T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159175454 | |||||||
chr6:159175666 | G | A | 27 | a0002c0004t0001g0164 a0002c0004t0001g0172 a0002c0004t0001g0176 others(24): Show |
28 | HG01109.hp1 HG01256.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.109+5961G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159175666 | |||||||
chr6:159175729 | T | C | 27 | a0002c0004t0001g0164 a0002c0004t0001g0172 a0002c0004t0001g0176 others(24): Show |
28 | HG01109.hp1 HG01256.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.109+6024T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159175729 | |||||||
chr6:159175781 | T | C | 27 | a0002c0004t0001g0164 a0002c0004t0001g0172 a0002c0004t0001g0176 others(24): Show |
28 | HG01109.hp1 HG01256.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.109+6076T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159175781 | |||||||
chr6:159175889 | C | T | 27 | a0002c0004t0001g0164 a0002c0004t0001g0172 a0002c0004t0001g0176 others(24): Show |
28 | HG01109.hp1 HG01256.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.109+6184C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159175889 | |||||||
chr6:159176008 | C | T | 1 | a0018c0047t0002g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.109+6303C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176008 | |||||||
chr6:159176249 | G | A | 4 | a0001c0005t0001g0287 a0001c0010t0003g0284 a0001c0010t0003g0286 others(1): Show |
4 | HG02622.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+6544G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176249 | |||||||
chr6:159176265 | G | T | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+6560G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176265 | |||||||
chr6:159176268 | C | CCATT | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+6579_109+6582d others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159176268 | ||||||
chr6:159176439 | A | G | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+6734A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176439 | |||||||
chr6:159176475 | T | A | 16 | a0002c0004t0001g0164 a0002c0004t0001g0172 a0002c0004t0001g0176 others(13): Show |
16 | HG01256.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.109+6770T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176475 | |||||||
chr6:159176530 | AC | A | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+6826delC | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176530 | |||||||
chr6:159176531 | C | T | 1 | a0001c0005t0001g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.109+6826C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176531 | |||||||
chr6:159176533 | T | A | 2 | a0004c0053t0003g0034 a0015c0030t0003g0033 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.109+6828T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176533 | |||||||
chr6:159176590 | A | G | 2 | a0032c0075t0002g0298 a0038c0076t0001g0299 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.109+6885A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176590 | |||||||
chr6:159176625 | G | A | 4 | a0003c0001t0002g0188 a0003c0012t0004g0185 a0003c0012t0004g0186 others(1): Show |
4 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+6920G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176625 | |||||||
chr6:159176793 | G | A | 1 | a0005c0002t0001g0069 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.109+7088G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176793 | |||||||
chr6:159176859 | T | C | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+7154T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176859 | |||||||
chr6:159176875 | T | G | 1 | a0002c0004t0001g0164 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.109+7170T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176875 | |||||||
chr6:159176949 | T | C | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+7244T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159176949 | |||||||
chr6:159177121 | A | G | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+7416A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177121 | |||||||
chr6:159177133 | G | T | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+7428G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177133 | |||||||
chr6:159177139 | A | G | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+7434A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177139 | |||||||
chr6:159177444 | A | T | 2 | a0004c0003t0002g0012 a0004c0003t0002g0068 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.109+7739A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177444 | |||||||
chr6:159177449 | C | T | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+7744C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177449 | |||||||
chr6:159177468 | G | A | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+7763G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177468 | |||||||
chr6:159177472 | G | A | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.109+7767G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177472 | |||||||
chr6:159177487 | G | A | 3 | a0001c0005t0001g0072 a0001c0006t0001g0070 a0001c0006t0001g0071 |
3 | HG01515.hp1 HG01517.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.109+7782G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177487 | |||||||
chr6:159177518 | G | A | 1 | a0018c0047t0002g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.109+7813G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177518 | |||||||
chr6:159177580 | C | CAGG | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+7878_109+7880d others(5): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159177580 | ||||||
chr6:159177599 | C | T | 132 | a0001c0006t0001g0141 a0002c0004t0001g0154 a0002c0004t0001g0164 others(129): Show |
133 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.109+7894C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177599 | |||||||
chr6:159177669 | C | T | 11 | a0002c0004t0001g0183 a0002c0017t0002g0005 a0002c0017t0002g0182 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+7964C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177669 | |||||||
chr6:159177702 | C | T | 1 | a0030c0064t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.109+7997C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177702 | |||||||
chr6:159177703 | G | A | 110 | a0001c0006t0001g0141 a0002c0004t0001g0154 a0002c0004t0001g0189 others(107): Show |
111 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.109+7998G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177703 | |||||||
chr6:159177821 | C | T | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.109+8116C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177821 | |||||||
chr6:159177822 | G | A | 29 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(26): Show |
30 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+8117G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177822 | |||||||
chr6:159177848 | T | C | 4 | a0001c0005t0001g0142 a0004c0053t0003g0034 a0015c0030t0003g0033 others(1): Show |
4 | HG01934.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+8143T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177848 | |||||||
chr6:159177863 | T | C | 1 | a0001c0006t0001g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.109+8158T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177863 | |||||||
chr6:159177877 | C | T | 2 | a0004c0068t0004g0149 a0005c0002t0001g0150 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.109+8172C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159177877 | |||||||
chr6:159178166 | C | T | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.109+8461C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159178166 | |||||||
chr6:159178243 | C | G | 1 | a0001c0006t0001g0141 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.109+8538C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159178243 | |||||||
chr6:159178271 | G | T | 1 | a0003c0001t0002g0279 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.109+8566G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159178271 | |||||||
chr6:159178302 | C | T | 1 | a0021c0050t0001g0278 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.109+8597C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159178302 | |||||||
chr6:159178424 | C | T | 1 | a0030c0064t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.109+8719C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159178424 | |||||||
chr6:159178429 | C | A | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.109+8724C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159178429 | |||||||
chr6:159178753 | T | G | 4 | a0012c0016t0002g0166 a0012c0016t0002g0168 a0028c0036t0003g0165 others(1): Show |
4 | HG02723.hp1 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+9048T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159178753 | |||||||
chr6:159178911 | A | G | 1 | a0005c0002t0001g0151 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.109+9206A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159178911 | |||||||
chr6:159178920 | A | G | 197 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(194): Show |
200 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.109+9215A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159178920 | |||||||
chr6:159179042 | C | T | 4 | a0005c0002t0001g0030 a0009c0013t0002g0029 a0009c0013t0002g0031 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+9337C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159179042 | |||||||
chr6:159179437 | T | G | 100 | a0001c0005t0001g0015 a0001c0005t0001g0072 a0001c0005t0001g0073 others(97): Show |
104 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.109+9732T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159179437 | |||||||
chr6:159179440 | C | T | 3 | a0003c0001t0002g0277 a0006c0007t0001g0153 a0021c0050t0001g0278 |
3 | HG00673.hp1 NA18969.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.109+9735C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159179440 | |||||||
chr6:159179488 | G | A | 2 | a0001c0005t0001g0142 a0026c0041t0002g0155 |
2 | HG01934.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.109+9783G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159179488 | |||||||
chr6:159179641 | C | T | 14 | a0001c0005t0001g0139 a0001c0005t0006g0137 a0001c0006t0001g0143 others(11): Show |
14 | HG00280.hp2 HG00621.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+9936C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159179641 | |||||||
chr6:159179699 | A | G | 1 | a0008c0070t0005g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.109+9994A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159179699 | |||||||
chr6:159179707 | C | T | 1 | a0005c0002t0001g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.109+10002C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159179707 | |||||||
chr6:159179958 | C | T | 1 | a0001c0010t0003g0022 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.109+10253C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159179958 | |||||||
chr6:159180288 | C | T | 1 | a0005c0002t0001g0067 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.109+10583C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159180288 | |||||||
chr6:159180425 | C | T | 1 | a0001c0010t0003g0128 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.109+10720C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159180425 | |||||||
chr6:159180553 | T | C | 3 | a0002c0004t0001g0189 a0003c0001t0002g0156 a0013c0024t0001g0190 |
3 | HG00544.hp2 NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.109+10848T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159180553 | |||||||
chr6:159180664 | G | C | 31 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(28): Show |
32 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.109+10959G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159180664 | |||||||
chr6:159180748 | C | T | 1 | a0004c0003t0002g0127 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.109+11043C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159180748 | |||||||
chr6:159180749 | T | C | 3 | a0005c0002t0001g0038 a0005c0002t0001g0039 a0016c0054t0003g0037 |
3 | HG02615.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109+11044T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159180749 | |||||||
chr6:159180838 | C | T | 17 | a0001c0005t0001g0287 a0001c0010t0003g0284 a0001c0010t0003g0286 others(14): Show |
18 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.109+11133C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159180838 | |||||||
chr6:159180943 | C | T | 1 | a0023c0044t0001g0296 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.109+11238C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159180943 | |||||||
chr6:159180947 | T | C | 2 | a0005c0002t0001g0030 a0009c0013t0002g0029 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.109+11242T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159180947 | |||||||
chr6:159181199 | T | C | 7 | a0002c0004t0001g0162 a0002c0021t0001g0169 a0002c0021t0001g0170 others(4): Show |
7 | HG02055.hp2 HG02630.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+11494T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159181199 | |||||||
chr6:159181454 | C | T | 2 | a0001c0005t0001g0287 a0001c0010t0003g0286 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.109+11749C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159181454 | |||||||
chr6:159181484 | T | C | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.109+11779T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159181484 | |||||||
chr6:159181503 | A | G | 1 | a0001c0006t0001g0148 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.109+11798A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159181503 | |||||||
chr6:159181532 | A | G | 15 | a0001c0005t0001g0139 a0001c0005t0006g0137 a0001c0006t0001g0126 others(12): Show |
15 | HG00280.hp2 HG00621.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.109+11827A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159181532 | |||||||
chr6:159181567 | A | G | 2 | a0004c0053t0003g0034 a0015c0030t0003g0033 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.109+11862A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159181567 | |||||||
chr6:159181684 | G | A | 4 | a0002c0004t0001g0162 a0006c0007t0001g0161 a0012c0037t0002g0160 others(1): Show |
4 | HG02055.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+11979G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159181684 | |||||||
chr6:159181967 | A | G | 1 | a0035c0060t0001g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.109+12262A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159181967 | |||||||
chr6:159181969 | T | C | 182 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(179): Show |
188 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.109+12264T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159181969 | |||||||
chr6:159182103 | C | T | 18 | a0001c0005t0001g0287 a0001c0010t0003g0284 a0001c0010t0003g0286 others(15): Show |
19 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.109+12398C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159182103 | |||||||
chr6:159182134 | C | T | 36 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(33): Show |
37 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.109+12429C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159182134 | |||||||
chr6:159182211 | T | A | 2 | a0002c0021t0001g0169 a0002c0021t0001g0170 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.109+12506T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159182211 | |||||||
chr6:159182385 | T | A | 1 | a0001c0005t0001g0073 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.109+12680T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159182385 | |||||||
chr6:159182468 | T | C | 20 | a0001c0005t0001g0287 a0001c0010t0003g0284 a0001c0010t0003g0286 others(17): Show |
21 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.109+12763T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159182468 | |||||||
chr6:159182690 | G | C | 96 | a0001c0005t0001g0015 a0001c0005t0001g0072 a0001c0005t0001g0073 others(93): Show |
100 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.109+12985G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159182690 | |||||||
chr6:159182926 | T | C | 105 | a0001c0005t0001g0015 a0001c0005t0001g0072 a0001c0005t0001g0073 others(102): Show |
109 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.109+13221T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159182926 | |||||||
chr6:159183320 | G | T | 85 | a0001c0005t0001g0015 a0001c0005t0001g0139 a0001c0005t0001g0142 others(82): Show |
90 | HG00280.hp2 HG00544.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.109+13615G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183320 | |||||||
chr6:159183353 | C | G | 1 | a0001c0033t0001g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.109+13648C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183353 | |||||||
chr6:159183363 | G | A | 3 | a0001c0005t0001g0072 a0001c0006t0001g0070 a0001c0006t0001g0071 |
3 | HG01515.hp1 HG01517.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.109+13658G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183363 | |||||||
chr6:159183388 | A | T | 10 | a0001c0006t0001g0018 a0001c0006t0001g0020 a0001c0006t0001g0146 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+13683A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183388 | |||||||
chr6:159183429 | C | T | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.109+13724C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183429 | |||||||
chr6:159183739 | T | C | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.110-13692T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183739 | |||||||
chr6:159183741 | G | A | 2 | a0002c0008t0001g0204 a0003c0001t0002g0203 |
2 | HG04228.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.110-13690G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183741 | |||||||
chr6:159183779 | G | A | 76 | a0001c0005t0001g0015 a0001c0005t0001g0075 a0001c0005t0001g0142 others(73): Show |
79 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.110-13652G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183779 | |||||||
chr6:159183793 | C | T | 2 | a0001c0005t0001g0287 a0001c0010t0003g0286 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.110-13638C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183793 | |||||||
chr6:159183865 | T | C | 1 | a0004c0003t0002g0129 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.110-13566T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183865 | |||||||
chr6:159183884 | G | A | 1 | a0017c0025t0001g0200 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.110-13547G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183884 | |||||||
chr6:159183908 | A | G | 2 | a0003c0001t0002g0178 a0008c0070t0005g0036 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.110-13523A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183908 | |||||||
chr6:159183956 | T | C | 28 | a0001c0005t0001g0079 a0001c0006t0001g0004 a0001c0010t0003g0013 others(25): Show |
30 | HG00140.hp1 HG00639.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.110-13475T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159183956 | |||||||
chr6:159184026 | T | C | 2 | a0003c0001t0002g0280 a0003c0001t0002g0281 |
2 | NA18974.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.110-13405T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184026 | |||||||
chr6:159184199 | T | A | 1 | a0009c0032t0003g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.110-13232T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184199 | |||||||
chr6:159184207 | T | G | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.110-13224T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184207 | |||||||
chr6:159184223 | C | T | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.110-13208C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184223 | |||||||
chr6:159184368 | C | T | 2 | a0001c0005t0001g0287 a0001c0010t0003g0286 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.110-13063C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184368 | |||||||
chr6:159184416 | C | A | 21 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0010t0003g0013 others(18): Show |
21 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.110-13015C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184416 | |||||||
chr6:159184502 | G | A | 1 | a0003c0001t0002g0276 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.110-12929G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184502 | |||||||
chr6:159184580 | C | T | 1 | a0008c0011t0003g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.110-12851C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184580 | |||||||
chr6:159184627 | G | T | 2 | a0005c0002t0001g0121 a0005c0002t0001g0122 |
2 | NA18987.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.110-12804G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184627 | |||||||
chr6:159184630 | G | A | 2 | a0005c0002t0001g0121 a0005c0002t0001g0122 |
2 | NA18987.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.110-12801G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184630 | |||||||
chr6:159184631 | C | A | 2 | a0005c0002t0001g0121 a0005c0002t0001g0122 |
2 | NA18987.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.110-12800C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184631 | |||||||
chr6:159184632 | T | A | 2 | a0005c0002t0001g0121 a0005c0002t0001g0122 |
2 | NA18987.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.110-12799T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184632 | |||||||
chr6:159184787 | C | T | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.110-12644C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184787 | |||||||
chr6:159184845 | C | T | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.110-12586C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184845 | |||||||
chr6:159184858 | G | A | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.110-12573G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159184858 | |||||||
chr6:159185067 | T | TG | 122 | a0001c0005t0001g0015 a0001c0005t0001g0050 a0001c0005t0001g0051 others(119): Show |
123 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.110-12353dupG | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159185067 | ||||||
chr6:159185067 | T | TGG | 60 | a0001c0005t0001g0082 a0001c0005t0001g0106 a0001c0005t0001g0139 others(57): Show |
61 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.110-12354_110-1235 others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159185067 | ||||||
chr6:159185071 | G | T | 4 | a0001c0005t0001g0072 a0001c0005t0001g0079 a0001c0006t0001g0111 others(1): Show |
4 | HG01175.hp2 HG01361.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-12360G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185071 | |||||||
chr6:159185076 | G | C | 3 | a0003c0001t0002g0178 a0003c0001t0002g0180 a0026c0041t0002g0155 |
3 | HG02109.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.110-12355G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185076 | |||||||
chr6:159185079 | A | G | 1 | a0001c0006t0001g0071 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.110-12352A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185079 | |||||||
chr6:159185094 | C | T | 1 | a0002c0008t0001g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.110-12337C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185094 | |||||||
chr6:159185118 | C | G | 1 | a0002c0018t0004g0175 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110-12313C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185118 | |||||||
chr6:159185393 | A | C | 1 | a0031c0040t0002g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.110-12038A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185393 | |||||||
chr6:159185714 | C | A | 1 | a0001c0062t0001g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.110-11717C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185714 | |||||||
chr6:159185730 | C | A | 4 | a0009c0032t0003g0288 a0012c0016t0002g0166 a0012c0016t0002g0168 others(1): Show |
4 | HG02976.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-11701C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185730 | |||||||
chr6:159185800 | G | T | 2 | a0009c0013t0002g0029 a0009c0013t0002g0031 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.110-11631G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185800 | |||||||
chr6:159185841 | T | C | 188 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(185): Show |
191 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.110-11590T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185841 | |||||||
chr6:159185950 | G | T | 158 | a0001c0005t0006g0137 a0002c0004t0001g0162 a0002c0004t0001g0183 others(155): Show |
161 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.110-11481G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159185950 | |||||||
chr6:159186071 | A | G | 3 | a0001c0005t0001g0093 a0001c0005t0001g0094 a0001c0005t0001g0098 |
3 | HG00733.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.110-11360A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159186071 | |||||||
chr6:159186235 | T | C | 2 | a0009c0013t0002g0029 a0009c0013t0002g0031 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.110-11196T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159186235 | |||||||
chr6:159186283 | T | C | 2 | a0002c0004t0001g0162 a0002c0004t0001g0183 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.110-11148T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159186283 | |||||||
chr6:159186563 | C | A | 9 | a0003c0001t0002g0178 a0003c0001t0002g0180 a0003c0045t0001g0192 others(6): Show |
9 | HG01109.hp1 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.110-10868C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159186563 | |||||||
chr6:159186746 | C | T | 7 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(4): Show |
7 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-10685C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159186746 | |||||||
chr6:159186896 | T | C | 1 | a0002c0004t0001g0154 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.110-10535T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159186896 | |||||||
chr6:159186970 | C | T | 1 | a0002c0008t0001g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.110-10461C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159186970 | |||||||
chr6:159187009 | C | T | 23 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0006t0001g0053 others(20): Show |
23 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.110-10422C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159187009 | |||||||
chr6:159187114 | C | G | 1 | a0002c0004t0001g0212 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.110-10317C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159187114 | |||||||
chr6:159187220 | A | G | 1 | a0002c0008t0001g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.110-10211A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159187220 | |||||||
chr6:159187270 | G | A | 2 | a0003c0001t0002g0178 a0003c0001t0002g0180 |
2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.110-10161G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159187270 | |||||||
chr6:159187514 | C | G | 1 | a0018c0047t0002g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.110-9917C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159187514 | |||||||
chr6:159187673 | A | C | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.110-9758A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159187673 | |||||||
chr6:159187916 | G | A | 2 | a0014c0027t0001g0077 a0014c0027t0001g0078 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.110-9515G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159187916 | |||||||
chr6:159187949 | C | T | 53 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(50): Show |
53 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.110-9482C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159187949 | |||||||
chr6:159188081 | A | C | 1 | a0004c0003t0002g0010 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.110-9350A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188081 | |||||||
chr6:159188124 | C | T | 1 | a0031c0040t0002g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.110-9307C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188124 | |||||||
chr6:159188154 | A | C | 5 | a0001c0006t0001g0018 a0002c0008t0001g0199 a0002c0008t0001g0235 others(2): Show |
5 | HG01074.hp2 HG01978.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-9277A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188154 | |||||||
chr6:159188222 | A | C | 7 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(4): Show |
7 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-9209A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188222 | |||||||
chr6:159188369 | C | A | 2 | a0001c0005t0001g0287 a0001c0010t0003g0286 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.110-9062C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188369 | |||||||
chr6:159188369 | C | CT | 12 | a0001c0005t0001g0048 a0001c0005t0001g0093 a0001c0005t0001g0094 others(9): Show |
13 | HG00733.hp2 HG00738.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.110-9039dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159188369 | ||||||
chr6:159188369 | CTTTTTTT others(2): Show |
C | 15 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(12): Show |
15 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-9047_110-9039d others(11): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159188369 | ||||||
chr6:159188369 | CTTTTTTT others(3): Show |
C | 172 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(169): Show |
175 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.110-9048_110-9039d others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159188369 | ||||||
chr6:159188369 | CTTTTTTT others(4): Show |
C | 1 | a0005c0002t0001g0067 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.110-9049_110-9039d others(13): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159188369 | ||||||
chr6:159188370 | T | A | 2 | a0001c0005t0001g0287 a0001c0010t0003g0286 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.110-9061T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188370 | |||||||
chr6:159188405 | T | C | 190 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(187): Show |
193 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.110-9026T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188405 | |||||||
chr6:159188537 | G | A | 12 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(9): Show |
12 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.110-8894G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188537 | |||||||
chr6:159188541 | A | AT | 10 | a0001c0005t0001g0093 a0001c0005t0001g0094 a0001c0005t0001g0098 others(7): Show |
10 | HG00733.hp1 HG00733.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-8880dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159188541 | ||||||
chr6:159188670 | G | A | 3 | a0001c0010t0003g0043 a0008c0070t0005g0036 a0026c0041t0002g0155 |
3 | HG02109.hp2 HG02738.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.110-8761G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188670 | |||||||
chr6:159188678 | G | A | 1 | a0001c0005t0001g0139 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.110-8753G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188678 | |||||||
chr6:159188746 | C | CT | 8 | a0001c0005t0001g0142 a0001c0006t0001g0020 a0001c0062t0001g0083 others(5): Show |
8 | HG01081.hp2 HG01256.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-8666dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159188746 | ||||||
chr6:159188746 | CT | C | 20 | a0002c0004t0001g0154 a0002c0004t0007g0208 a0003c0001t0002g0178 others(17): Show |
20 | HG01069.hp2 HG01109.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.110-8666delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 159188746 | ||||||
chr6:159188826 | C | T | 2 | a0001c0010t0003g0074 a0001c0010t0003g0128 |
2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.110-8605C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188826 | |||||||
chr6:159188834 | G | A | 1 | a0003c0001t0002g0213 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.110-8597G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188834 | |||||||
chr6:159188851 | G | A | 59 | a0003c0001t0002g0006 a0003c0001t0002g0188 a0003c0001t0002g0191 others(56): Show |
60 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.110-8580G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188851 | |||||||
chr6:159188926 | A | G | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.110-8505A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159188926 | |||||||
chr6:159189037 | C | T | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-8394C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189037 | |||||||
chr6:159189072 | A | G | 3 | a0016c0031t0003g0289 a0016c0054t0003g0037 a0028c0036t0003g0165 |
3 | HG02723.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.110-8359A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189072 | |||||||
chr6:159189135 | G | T | 32 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(29): Show |
32 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.110-8296G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189135 | |||||||
chr6:159189328 | G | A | 1 | a0008c0070t0005g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.110-8103G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189328 | |||||||
chr6:159189447 | G | A | 1 | a0006c0007t0001g0273 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.110-7984G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189447 | |||||||
chr6:159189502 | T | C | 3 | a0003c0001t0002g0178 a0003c0001t0002g0180 a0026c0041t0002g0155 |
3 | HG02109.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.110-7929T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189502 | |||||||
chr6:159189558 | A | G | 2 | a0001c0006t0001g0020 a0001c0006t0001g0143 |
2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.110-7873A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189558 | |||||||
chr6:159189590 | C | T | 163 | a0001c0005t0006g0137 a0001c0055t0003g0062 a0002c0004t0001g0162 others(160): Show |
166 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.110-7841C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189590 | |||||||
chr6:159189685 | C | T | 5 | a0001c0055t0003g0062 a0004c0069t0001g0007 a0005c0002t0001g0150 others(2): Show |
5 | HG02622.hp1 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-7746C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189685 | |||||||
chr6:159189737 | G | A | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.110-7694G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189737 | |||||||
chr6:159189832 | G | A | 1 | a0024c0073t0003g0011 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.110-7599G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189832 | |||||||
chr6:159189872 | T | C | 135 | a0001c0005t0006g0137 a0002c0004t0001g0162 a0002c0004t0001g0183 others(132): Show |
138 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.110-7559T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189872 | |||||||
chr6:159189914 | C | T | 163 | a0001c0005t0006g0137 a0001c0055t0003g0062 a0002c0004t0001g0162 others(160): Show |
166 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.110-7517C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159189914 | |||||||
chr6:159190015 | T | C | 1 | a0005c0015t0001g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110-7416T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159190015 | |||||||
chr6:159190112 | A | G | 39 | a0001c0005t0006g0137 a0002c0004t0001g0162 a0002c0004t0001g0183 others(36): Show |
39 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.110-7319A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159190112 | |||||||
chr6:159190119 | C | T | 134 | a0001c0005t0006g0137 a0002c0004t0001g0162 a0002c0004t0001g0183 others(131): Show |
137 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.110-7312C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159190119 | |||||||
chr6:159190135 | G | A | 1 | a0008c0070t0005g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.110-7296G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159190135 | |||||||
chr6:159190149 | C | G | 1 | a0008c0028t0002g0055 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.110-7282C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159190149 | |||||||
chr6:159190233 | A | G | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.110-7198A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159190233 | |||||||
chr6:159190567 | T | C | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.110-6864T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159190567 | |||||||
chr6:159190737 | C | T | 2 | a0003c0001t0002g0178 a0003c0001t0002g0180 |
2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.110-6694C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159190737 | |||||||
chr6:159190811 | T | G | 2 | a0001c0006t0001g0020 a0001c0006t0001g0143 |
2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.110-6620T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159190811 | |||||||
chr6:159191010 | G | A | 1 | a0004c0003t0002g0112 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.110-6421G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191010 | |||||||
chr6:159191060 | G | A | 2 | a0003c0001t0002g0178 a0003c0001t0002g0180 |
2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.110-6371G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191060 | |||||||
chr6:159191085 | G | A | 1 | a0004c0003t0002g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.110-6346G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191085 | |||||||
chr6:159191228 | A | C | 9 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(6): Show |
9 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-6203A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191228 | |||||||
chr6:159191240 | G | A | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.110-6191G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191240 | |||||||
chr6:159191267 | A | G | 1 | a0030c0064t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.110-6164A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191267 | |||||||
chr6:159191318 | C | T | 7 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(4): Show |
7 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-6113C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191318 | |||||||
chr6:159191564 | A | G | 1 | a0003c0001t0002g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.110-5867A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191564 | |||||||
chr6:159191567 | T | C | 1 | a0001c0010t0003g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.110-5864T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191567 | |||||||
chr6:159191629 | A | G | 133 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0003c0001t0002g0006 others(130): Show |
136 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.110-5802A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191629 | |||||||
chr6:159191713 | C | G | 9 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(6): Show |
9 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-5718C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191713 | |||||||
chr6:159191823 | G | A | 2 | a0002c0004t0007g0208 a0003c0001t0002g0269 |
2 | HG01069.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.110-5608G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159191823 | |||||||
chr6:159192018 | C | T | 1 | a0022c0056t0001g0124 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.110-5413C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192018 | |||||||
chr6:159192026 | T | C | 2 | a0001c0063t0002g0285 a0012c0037t0002g0160 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.110-5405T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192026 | |||||||
chr6:159192075 | A | G | 7 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(4): Show |
7 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-5356A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192075 | |||||||
chr6:159192108 | G | A | 15 | a0001c0055t0003g0062 a0003c0012t0004g0171 a0003c0012t0004g0185 others(12): Show |
15 | HG01243.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-5323G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192108 | |||||||
chr6:159192158 | G | A | 147 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0002c0039t0002g0205 others(144): Show |
150 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.110-5273G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192158 | |||||||
chr6:159192245 | T | C | 15 | a0001c0055t0003g0062 a0003c0012t0004g0171 a0003c0012t0004g0185 others(12): Show |
15 | HG01243.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-5186T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192245 | |||||||
chr6:159192253 | C | T | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.110-5178C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192253 | |||||||
chr6:159192504 | C | T | 187 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(184): Show |
190 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.110-4927C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192504 | |||||||
chr6:159192512 | G | A | 133 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0003c0001t0002g0006 others(130): Show |
136 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.110-4919G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192512 | |||||||
chr6:159192517 | C | T | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.110-4914C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192517 | |||||||
chr6:159192780 | G | A | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.110-4651G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192780 | |||||||
chr6:159192869 | G | C | 15 | a0001c0055t0003g0062 a0003c0012t0004g0171 a0003c0012t0004g0185 others(12): Show |
15 | HG01243.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-4562G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192869 | |||||||
chr6:159192980 | C | T | 1 | a0004c0003t0002g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.110-4451C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159192980 | |||||||
chr6:159193295 | G | A | 6 | a0001c0055t0003g0062 a0004c0069t0001g0007 a0005c0002t0001g0150 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-4136G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159193295 | |||||||
chr6:159193367 | G | A | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.110-4064G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159193367 | |||||||
chr6:159193538 | A | G | 2 | a0005c0002t0001g0058 a0005c0002t0001g0091 |
2 | NA18947.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.110-3893A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159193538 | |||||||
chr6:159193588 | G | A | 14 | a0001c0055t0003g0062 a0003c0012t0004g0171 a0003c0012t0004g0185 others(11): Show |
14 | HG01243.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.110-3843G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159193588 | |||||||
chr6:159193857 | C | T | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.110-3574C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159193857 | |||||||
chr6:159193913 | C | A | 1 | a0008c0070t0005g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.110-3518C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159193913 | |||||||
chr6:159193963 | T | G | 1 | a0001c0006t0001g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110-3468T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159193963 | |||||||
chr6:159194366 | T | C | 6 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(3): Show |
6 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-3065T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159194366 | |||||||
chr6:159194537 | T | C | 1 | a0004c0003t0002g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.110-2894T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159194537 | |||||||
chr6:159194847 | G | T | 22 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0006t0001g0053 others(19): Show |
22 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.110-2584G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159194847 | |||||||
chr6:159195059 | G | A | 2 | a0002c0017t0002g0005 a0002c0017t0002g0182 |
3 | HG02559.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.110-2372G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159195059 | |||||||
chr6:159195139 | G | A | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.110-2292G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159195139 | |||||||
chr6:159195234 | T | G | 2 | a0009c0013t0002g0029 a0009c0013t0002g0031 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.110-2197T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159195234 | |||||||
chr6:159195643 | C | G | 189 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(186): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.110-1788C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159195643 | |||||||
chr6:159195710 | G | C | 2 | a0003c0001t0002g0188 a0004c0003t0002g0068 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.110-1721G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159195710 | |||||||
chr6:159195821 | T | A | 1 | a0002c0008t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.110-1610T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159195821 | |||||||
chr6:159195882 | A | G | 1 | a0001c0006t0001g0111 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.110-1549A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159195882 | |||||||
chr6:159195974 | C | T | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110-1457C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159195974 | |||||||
chr6:159196282 | C | G | 1 | a0003c0001t0002g0281 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.110-1149C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159196282 | |||||||
chr6:159196824 | T | G | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.110-607T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159196824 | |||||||
chr6:159197022 | T | C | 5 | a0001c0055t0003g0062 a0004c0069t0001g0007 a0005c0002t0001g0150 others(2): Show |
5 | HG02622.hp1 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-409T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159197022 | |||||||
chr6:159197062 | C | T | 1 | a0004c0003t0002g0017 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.110-369C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159197062 | |||||||
chr6:159197115 | C | T | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110-316C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159197115 | |||||||
chr6:159197243 | T | C | 7 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(4): Show |
7 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-188T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159197243 | |||||||
chr6:159197253 | A | G | 15 | a0001c0055t0003g0062 a0003c0012t0004g0171 a0003c0012t0004g0185 others(12): Show |
15 | HG01243.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-178A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159197253 | |||||||
chr6:159197270 | A | G | 1 | a0008c0028t0002g0055 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.110-161A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159197270 | |||||||
chr6:159197271 | C | T | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.110-160C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159197271 | |||||||
chr6:159197333 | G | A | 4 | a0001c0006t0001g0141 a0001c0006t0001g0146 a0001c0006t0001g0147 others(1): Show |
4 | HG01256.hp2 HG01361.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-98G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159197333 | |||||||
chr6:159197365 | C | T | 138 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0003c0001t0002g0006 others(135): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.110-66C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 1/22 | chr6 | 159197365 | |||||||
chr6:159197758 | G | A | 138 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0003c0001t0002g0006 others(135): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.304+133G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159197758 | |||||||
chr6:159197780 | G | A | 2 | a0001c0063t0002g0285 a0012c0037t0002g0160 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.304+155G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159197780 | |||||||
chr6:159197784 | G | A | 7 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(4): Show |
7 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+159G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159197784 | |||||||
chr6:159198023 | C | T | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.304+398C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198023 | |||||||
chr6:159198259 | C | T | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.304+634C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198259 | |||||||
chr6:159198336 | C | A | 2 | a0006c0026t0001g0252 a0006c0026t0001g0253 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.304+711C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198336 | |||||||
chr6:159198339 | T | C | 1 | a0009c0032t0003g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.304+714T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198339 | |||||||
chr6:159198470 | CA | C | 8 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(5): Show |
8 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.304+846delA | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198470 | |||||||
chr6:159198545 | TA | T | 8 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(5): Show |
8 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.304+922delA | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 159198545 | ||||||
chr6:159198558 | G | A | 190 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(187): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.304+933G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198558 | |||||||
chr6:159198638 | T | G | 1 | a0001c0010t0003g0286 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.304+1013T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198638 | |||||||
chr6:159198773 | A | G | 7 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(4): Show |
7 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+1148A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198773 | |||||||
chr6:159198834 | G | A | 138 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0003c0001t0002g0006 others(135): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.305-1162G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198834 | |||||||
chr6:159198893 | G | A | 1 | a0028c0036t0003g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.305-1103G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198893 | |||||||
chr6:159198972 | G | C | 1 | a0001c0006t0001g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.305-1024G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159198972 | |||||||
chr6:159199238 | C | T | 3 | a0001c0033t0001g0295 a0002c0021t0001g0169 a0002c0021t0001g0170 |
3 | HG02630.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.305-758C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159199238 | |||||||
chr6:159199287 | C | T | 1 | a0012c0037t0002g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.305-709C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159199287 | |||||||
chr6:159199478 | A | G | 190 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(187): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.305-518A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159199478 | |||||||
chr6:159199510 | T | C | 3 | a0005c0002t0001g0150 a0006c0007t0001g0179 a0038c0076t0001g0299 |
3 | HG02723.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.305-486T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159199510 | |||||||
chr6:159199646 | C | G | 4 | a0003c0001t0002g0268 a0004c0003t0002g0113 a0004c0003t0002g0114 others(1): Show |
4 | HG00544.hp1 NA18953.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.305-350C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159199646 | |||||||
chr6:159199753 | T | C | 2 | a0029c0058t0001g0080 a0034c0038t0002g0152 |
2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.305-243T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159199753 | |||||||
chr6:159199868 | C | T | 1 | a0004c0003t0002g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.305-128C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159199868 | |||||||
chr6:159199893 | G | A | 137 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0003c0001t0002g0006 others(134): Show |
140 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.305-103G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159199893 | |||||||
chr6:159199960 | C | G | 1 | a0005c0015t0001g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.305-36C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 2/22 | chr6 | 159199960 | |||||||
chr6:159200302 | T | C | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.392-211T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 3/22 | chr6 | 159200302 | |||||||
chr6:159200653 | G | A | 5 | a0003c0001t0002g0216 a0003c0001t0002g0269 a0003c0022t0001g0248 others(2): Show |
5 | NA18965.hp2 NA18989.hp2 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.460+72G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159200653 | |||||||
chr6:159200780 | A | G | 1 | a0003c0001t0002g0198 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.460+199A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159200780 | |||||||
chr6:159200994 | A | G | 190 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(187): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.460+413A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159200994 | |||||||
chr6:159201234 | T | C | 3 | a0002c0018t0003g0219 a0002c0018t0003g0220 a0003c0001t0002g0277 |
3 | HG00140.hp1 HG00639.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.460+653T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159201234 | |||||||
chr6:159201326 | A | C | 1 | a0005c0002t0001g0060 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.460+745A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159201326 | |||||||
chr6:159201354 | A | G | 6 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(3): Show |
6 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.460+773A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159201354 | |||||||
chr6:159201361 | A | G | 190 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(187): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.460+780A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159201361 | |||||||
chr6:159201677 | A | G | 1 | a0031c0040t0002g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.460+1096A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159201677 | |||||||
chr6:159201769 | C | T | 8 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(5): Show |
8 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.460+1188C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159201769 | |||||||
chr6:159201770 | G | A | 152 | a0001c0005t0001g0142 a0001c0005t0006g0137 a0001c0055t0003g0062 others(149): Show |
155 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.460+1189G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159201770 | |||||||
chr6:159201793 | G | A | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.460+1212G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159201793 | |||||||
chr6:159201865 | C | G | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.460+1284C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159201865 | |||||||
chr6:159202173 | A | G | 1 | a0003c0001t0002g0280 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.460+1592A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159202173 | |||||||
chr6:159202245 | A | T | 4 | a0009c0032t0003g0288 a0012c0016t0002g0166 a0012c0016t0002g0168 others(1): Show |
4 | HG02976.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.460+1664A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159202245 | |||||||
chr6:159202464 | C | G | 2 | a0003c0001t0002g0178 a0003c0001t0002g0180 |
2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.460+1883C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159202464 | |||||||
chr6:159202629 | A | G | 2 | a0003c0001t0002g0156 a0003c0001t0002g0207 |
2 | HG02300.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.460+2048A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159202629 | |||||||
chr6:159202952 | G | T | 8 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(5): Show |
8 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.460+2371G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159202952 | |||||||
chr6:159203041 | T | C | 20 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0006t0001g0053 others(17): Show |
20 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.460+2460T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159203041 | |||||||
chr6:159203317 | C | T | 1 | a0004c0003t0002g0113 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.460+2736C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159203317 | |||||||
chr6:159203381 | G | A | 1 | a0002c0004t0001g0238 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.460+2800G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159203381 | |||||||
chr6:159203423 | A | T | 1 | a0001c0006t0001g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.460+2842A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159203423 | |||||||
chr6:159203450 | A | T | 1 | a0005c0002t0001g0120 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.460+2869A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159203450 | |||||||
chr6:159203648 | G | A | 181 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(178): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.460+3067G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159203648 | |||||||
chr6:159203703 | A | T | 1 | a0004c0034t0004g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.460+3122A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159203703 | |||||||
chr6:159203956 | C | A | 1 | a0003c0012t0004g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.460+3375C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159203956 | |||||||
chr6:159204084 | G | A | 8 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(5): Show |
8 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.460+3503G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204084 | |||||||
chr6:159204114 | A | C | 1 | a0003c0001t0002g0233 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.460+3533A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204114 | |||||||
chr6:159204180 | G | A | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.460+3599G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204180 | |||||||
chr6:159204306 | A | G | 1 | a0001c0006t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.460+3725A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204306 | |||||||
chr6:159204357 | A | C | 5 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.460+3776A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204357 | |||||||
chr6:159204368 | G | C | 1 | a0002c0017t0002g0182 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.460+3787G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204368 | |||||||
chr6:159204517 | G | A | 1 | a0003c0001t0002g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.460+3936G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204517 | |||||||
chr6:159204531 | G | A | 5 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.460+3950G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204531 | |||||||
chr6:159204614 | G | T | 182 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(179): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.460+4033G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204614 | |||||||
chr6:159204771 | C | T | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.460+4190C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204771 | |||||||
chr6:159204777 | C | T | 2 | a0005c0002t0001g0058 a0005c0002t0001g0091 |
2 | NA18947.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.460+4196C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204777 | |||||||
chr6:159204802 | C | G | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.460+4221C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204802 | |||||||
chr6:159204993 | C | G | 1 | a0010c0014t0003g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.460+4412C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159204993 | |||||||
chr6:159205040 | C | T | 138 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0003c0001t0002g0006 others(135): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.460+4459C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205040 | |||||||
chr6:159205059 | A | G | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.460+4478A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205059 | |||||||
chr6:159205190 | C | T | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.460+4609C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205190 | |||||||
chr6:159205460 | C | T | 4 | a0009c0032t0003g0288 a0012c0016t0002g0166 a0012c0016t0002g0168 others(1): Show |
4 | HG02976.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.460+4879C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205460 | |||||||
chr6:159205493 | C | T | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.460+4912C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205493 | |||||||
chr6:159205523 | C | T | 182 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(179): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.460+4942C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205523 | |||||||
chr6:159205548 | G | C | 8 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(5): Show |
8 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.460+4967G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205548 | |||||||
chr6:159205621 | A | G | 6 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(3): Show |
6 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.460+5040A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205621 | |||||||
chr6:159205711 | A | T | 190 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(187): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.460+5130A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205711 | |||||||
chr6:159205930 | G | A | 9 | a0005c0002t0001g0003 a0005c0002t0001g0027 a0005c0002t0001g0028 others(6): Show |
10 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.460+5349G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205930 | |||||||
chr6:159205951 | TC | T | 3 | a0016c0031t0003g0289 a0016c0054t0003g0037 a0028c0036t0003g0165 |
3 | HG02723.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.460+5374delC | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159205951 | ||||||
chr6:159205998 | G | T | 30 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(27): Show |
30 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.460+5417G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159205998 | |||||||
chr6:159206045 | C | T | 138 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0003c0001t0002g0006 others(135): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.460+5464C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159206045 | |||||||
chr6:159206148 | C | G | 4 | a0009c0032t0003g0288 a0012c0016t0002g0166 a0012c0016t0002g0168 others(1): Show |
4 | HG02976.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.460+5567C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159206148 | |||||||
chr6:159206591 | G | A | 1 | a0005c0015t0001g0291 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.460+6010G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159206591 | |||||||
chr6:159206760 | T | C | 2 | a0009c0013t0002g0029 a0009c0013t0002g0031 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.460+6179T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159206760 | |||||||
chr6:159206820 | C | A | 1 | a0003c0001t0002g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.460+6239C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159206820 | |||||||
chr6:159206823 | C | A | 1 | a0031c0040t0002g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.460+6242C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159206823 | |||||||
chr6:159207108 | C | G | 1 | a0003c0001t0002g0246 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.460+6527C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159207108 | |||||||
chr6:159207229 | A | G | 190 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(187): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.460+6648A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159207229 | |||||||
chr6:159207318 | C | T | 1 | a0031c0040t0002g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.460+6737C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159207318 | |||||||
chr6:159207496 | T | C | 5 | a0001c0055t0003g0062 a0004c0069t0001g0007 a0005c0002t0001g0150 others(2): Show |
5 | HG02622.hp1 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.460+6915T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159207496 | |||||||
chr6:159207581 | G | A | 41 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0005c0002t0001g0014 others(38): Show |
41 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.460+7000G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159207581 | |||||||
chr6:159207763 | T | G | 2 | a0003c0001t0002g0178 a0003c0001t0002g0180 |
2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.460+7182T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159207763 | |||||||
chr6:159207854 | C | A | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.461-7091C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159207854 | |||||||
chr6:159207918 | C | T | 1 | a0030c0064t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.461-7027C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159207918 | |||||||
chr6:159207946 | G | A | 181 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(178): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.461-6999G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159207946 | |||||||
chr6:159208013 | C | G | 33 | a0004c0034t0004g0294 a0005c0002t0001g0003 a0005c0002t0001g0008 others(30): Show |
35 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.461-6932C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208013 | |||||||
chr6:159208254 | G | A | 2 | a0003c0001t0002g0178 a0003c0001t0002g0180 |
2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.461-6691G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208254 | |||||||
chr6:159208319 | G | C | 1 | a0001c0006t0001g0020 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.461-6626G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208319 | |||||||
chr6:159208374 | C | T | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.461-6571C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208374 | |||||||
chr6:159208410 | A | T | 5 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-6535A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208410 | |||||||
chr6:159208425 | G | A | 2 | a0003c0001t0002g0178 a0003c0001t0002g0180 |
2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.461-6520G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208425 | |||||||
chr6:159208539 | C | T | 1 | a0003c0012t0004g0171 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.461-6406C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208539 | |||||||
chr6:159208644 | C | T | 5 | a0002c0039t0002g0205 a0009c0032t0003g0288 a0012c0016t0002g0166 others(2): Show |
5 | HG02976.hp2 HG03195.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.461-6301C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208644 | |||||||
chr6:159208690 | T | A | 5 | a0005c0002t0001g0121 a0005c0002t0001g0122 a0006c0007t0001g0202 others(2): Show |
5 | HG02015.hp1 HG02523.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-6255T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208690 | |||||||
chr6:159208817 | T | C | 1 | a0004c0034t0004g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.461-6128T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208817 | |||||||
chr6:159208844 | A | AT | 7 | a0001c0005t0001g0090 a0002c0004t0001g0242 a0002c0008t0001g0261 others(4): Show |
7 | HG01175.hp1 HG02056.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.461-6081dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159208844 | ||||||
chr6:159208844 | A | ATT | 26 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0006t0001g0053 others(23): Show |
26 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.461-6082_461-6081d others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159208844 | ||||||
chr6:159208844 | A | ATTT | 24 | a0001c0005t0001g0142 a0003c0001t0002g0214 a0003c0001t0002g0246 others(21): Show |
24 | HG00673.hp1 HG01167.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.461-6083_461-6081d others(5): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159208844 | ||||||
chr6:159208844 | A | ATTTT | 119 | a0001c0005t0006g0137 a0001c0055t0003g0062 a0002c0008t0001g0283 others(116): Show |
122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.461-6084_461-6081d others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159208844 | ||||||
chr6:159208844 | A | ATTTTT | 11 | a0003c0001t0002g0267 a0003c0001t0002g0268 a0004c0003t0002g0104 others(8): Show |
11 | HG00621.hp1 HG00741.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.461-6085_461-6081d others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159208844 | ||||||
chr6:159208844 | AT | A | 8 | a0001c0033t0001g0295 a0002c0004t0001g0164 a0002c0004t0001g0209 others(5): Show |
8 | HG01169.hp2 HG01256.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.461-6081delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159208844 | ||||||
chr6:159208856 | T | C | 1 | a0001c0005t0001g0047 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.461-6089T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208856 | |||||||
chr6:159208923 | C | T | 2 | a0016c0031t0003g0289 a0028c0036t0003g0165 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.461-6022C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208923 | |||||||
chr6:159208924 | C | T | 12 | a0001c0055t0003g0062 a0003c0012t0004g0171 a0003c0012t0004g0185 others(9): Show |
12 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.461-6021C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159208924 | |||||||
chr6:159209074 | C | T | 1 | a0003c0001t0002g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.461-5871C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209074 | |||||||
chr6:159209145 | G | C | 195 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(192): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.461-5800G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209145 | |||||||
chr6:159209170 | C | T | 42 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0005c0002t0001g0014 others(39): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.461-5775C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209170 | |||||||
chr6:159209212 | T | G | 34 | a0004c0034t0004g0294 a0005c0002t0001g0003 a0005c0002t0001g0008 others(31): Show |
36 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.461-5733T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209212 | |||||||
chr6:159209254 | G | C | 69 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(66): Show |
70 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.461-5691G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209254 | |||||||
chr6:159209281 | T | G | 3 | a0007c0052t0003g0222 a0010c0014t0003g0019 a0024c0073t0003g0011 |
3 | HG01255.hp1 HG01257.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.461-5664T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209281 | |||||||
chr6:159209282 | C | T | 3 | a0007c0052t0003g0222 a0010c0014t0003g0019 a0024c0073t0003g0011 |
3 | HG01255.hp1 HG01257.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.461-5663C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209282 | |||||||
chr6:159209320 | C | A | 73 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0005c0002t0001g0003 others(70): Show |
75 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.461-5625C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209320 | |||||||
chr6:159209466 | C | A | 1 | a0004c0068t0004g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.461-5479C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209466 | |||||||
chr6:159209539 | T | A | 5 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(2): Show |
5 | HG02258.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.461-5406T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209539 | |||||||
chr6:159209575 | G | A | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.461-5370G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209575 | |||||||
chr6:159209587 | A | G | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.461-5358A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209587 | |||||||
chr6:159209814 | T | G | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.461-5131T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209814 | |||||||
chr6:159209907 | C | G | 121 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(118): Show |
123 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.461-5038C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209907 | |||||||
chr6:159209931 | C | T | 2 | a0006c0026t0001g0252 a0006c0026t0001g0253 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.461-5014C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159209931 | |||||||
chr6:159210069 | C | A | 3 | a0002c0039t0002g0205 a0015c0030t0003g0032 a0015c0030t0003g0033 |
3 | HG02258.hp2 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.461-4876C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210069 | |||||||
chr6:159210107 | G | T | 65 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(62): Show |
66 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.461-4838G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210107 | |||||||
chr6:159210123 | G | T | 1 | a0005c0002t0001g0089 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.461-4822G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210123 | |||||||
chr6:159210130 | C | T | 1 | a0002c0008t0001g0244 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.461-4815C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210130 | |||||||
chr6:159210145 | C | T | 65 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(62): Show |
66 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.461-4800C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210145 | |||||||
chr6:159210168 | T | C | 20 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(17): Show |
20 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.461-4777T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210168 | |||||||
chr6:159210299 | A | G | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.461-4646A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210299 | |||||||
chr6:159210307 | G | A | 7 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(4): Show |
7 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.461-4638G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210307 | |||||||
chr6:159210365 | C | A | 65 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(62): Show |
66 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.461-4580C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210365 | |||||||
chr6:159210561 | C | T | 1 | a0034c0038t0002g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.461-4384C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210561 | |||||||
chr6:159210603 | T | C | 4 | a0009c0032t0003g0288 a0012c0016t0002g0166 a0012c0016t0002g0168 others(1): Show |
4 | HG02976.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-4342T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210603 | |||||||
chr6:159210733 | G | A | 1 | a0003c0001t0002g0268 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.461-4212G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210733 | |||||||
chr6:159210822 | C | T | 120 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(117): Show |
122 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.461-4123C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210822 | |||||||
chr6:159210980 | C | T | 20 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(17): Show |
20 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.461-3965C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159210980 | |||||||
chr6:159211000 | T | G | 191 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(188): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.461-3945T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159211000 | |||||||
chr6:159211013 | C | T | 191 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(188): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.461-3932C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159211013 | |||||||
chr6:159211218 | T | C | 77 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0005c0002t0001g0003 others(74): Show |
79 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.461-3727T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159211218 | |||||||
chr6:159211421 | C | T | 4 | a0009c0032t0003g0288 a0012c0016t0002g0166 a0012c0016t0002g0168 others(1): Show |
4 | HG02976.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-3524C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159211421 | |||||||
chr6:159211661 | A | G | 1 | a0032c0075t0002g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.461-3284A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159211661 | |||||||
chr6:159211809 | A | G | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.461-3136A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159211809 | |||||||
chr6:159211962 | C | T | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.461-2983C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159211962 | |||||||
chr6:159212006 | T | C | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.461-2939T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159212006 | |||||||
chr6:159212101 | C | G | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.461-2844C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159212101 | |||||||
chr6:159212163 | C | T | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.461-2782C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159212163 | |||||||
chr6:159212223 | C | T | 1 | a0023c0044t0001g0296 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.461-2722C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159212223 | |||||||
chr6:159212334 | T | C | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.461-2611T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159212334 | |||||||
chr6:159212337 | G | C | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-2608G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159212337 | |||||||
chr6:159212532 | G | GA | 6 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-2406dupA | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159212532 | ||||||
chr6:159212568 | T | G | 121 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(118): Show |
123 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.461-2377T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159212568 | |||||||
chr6:159212635 | C | A | 1 | a0005c0015t0001g0291 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.461-2310C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159212635 | |||||||
chr6:159212636 | G | A | 2 | a0004c0019t0001g0116 a0017c0025t0001g0200 |
2 | NA18993.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.461-2309G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159212636 | |||||||
chr6:159212832 | G | A | 1 | a0003c0001t0002g0246 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.461-2113G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159212832 | |||||||
chr6:159213035 | C | T | 1 | a0001c0006t0001g0088 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.461-1910C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213035 | |||||||
chr6:159213110 | G | A | 77 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0005c0002t0001g0003 others(74): Show |
79 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.461-1835G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213110 | |||||||
chr6:159213199 | G | C | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-1746G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213199 | |||||||
chr6:159213293 | A | G | 4 | a0001c0005t0001g0072 a0001c0005t0001g0079 a0001c0006t0001g0111 others(1): Show |
4 | HG00738.hp1 HG01175.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-1652A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213293 | |||||||
chr6:159213312 | T | G | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.461-1633T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213312 | |||||||
chr6:159213568 | A | G | 1 | a0007c0009t0002g0257 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.461-1377A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213568 | |||||||
chr6:159213576 | A | G | 53 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(50): Show |
53 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.461-1369A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213576 | |||||||
chr6:159213634 | A | AT | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-1310dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159213634 | ||||||
chr6:159213642 | A | C | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.461-1303A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213642 | |||||||
chr6:159213701 | CA | C | 117 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(114): Show |
119 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.461-1231delA | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159213701 | ||||||
chr6:159213701 | CAA | C | 6 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-1232_461-1231d others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 159213701 | ||||||
chr6:159213704 | A | AC | 68 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(65): Show |
69 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.461-1241_461-1240i others(3): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213704 | |||||||
chr6:159213704 | A | C | 1 | a0003c0001t0002g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.461-1241A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213704 | |||||||
chr6:159213705 | A | C | 4 | a0001c0006t0001g0088 a0002c0008t0001g0204 a0009c0013t0002g0029 others(1): Show |
4 | HG01243.hp2 NA18980.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-1240A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213705 | |||||||
chr6:159213706 | A | C | 1 | a0007c0009t0002g0274 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.461-1239A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213706 | |||||||
chr6:159213707 | A | C | 1 | a0008c0011t0003g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.461-1238A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213707 | |||||||
chr6:159213870 | C | T | 1 | a0002c0018t0004g0175 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.461-1075C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213870 | |||||||
chr6:159213942 | G | A | 190 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(187): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.461-1003G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159213942 | |||||||
chr6:159214063 | G | A | 65 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(62): Show |
66 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.461-882G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159214063 | |||||||
chr6:159214090 | C | A | 8 | a0001c0055t0003g0062 a0003c0045t0001g0192 a0004c0020t0001g0099 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.461-855C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159214090 | |||||||
chr6:159214354 | T | C | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-591T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159214354 | |||||||
chr6:159214395 | G | A | 6 | a0003c0001t0002g0262 a0003c0043t0002g0197 a0003c0051t0002g0264 others(3): Show |
6 | HG00408.hp1 HG00438.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-550G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159214395 | |||||||
chr6:159214606 | T | G | 118 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(115): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.461-339T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159214606 | |||||||
chr6:159214609 | T | A | 195 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(192): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.461-336T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159214609 | |||||||
chr6:159214756 | A | G | 69 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(66): Show |
70 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.461-189A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159214756 | |||||||
chr6:159214911 | T | G | 77 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0005c0002t0001g0003 others(74): Show |
79 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.461-34T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 4/22 | chr6 | 159214911 | |||||||
chr6:159215228 | A | G | 1 | a0018c0047t0002g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.667+77A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215228 | |||||||
chr6:159215284 | A | G | 1 | a0008c0011t0003g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.667+133A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215284 | |||||||
chr6:159215323 | A | T | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.667+172A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215323 | |||||||
chr6:159215346 | G | A | 75 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(72): Show |
76 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.667+195G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215346 | |||||||
chr6:159215409 | G | A | 7 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(4): Show |
7 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.667+258G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215409 | |||||||
chr6:159215444 | G | A | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.667+293G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215444 | |||||||
chr6:159215488 | T | C | 6 | a0003c0001t0002g0262 a0003c0043t0002g0197 a0003c0051t0002g0264 others(3): Show |
6 | HG00408.hp1 HG00438.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.667+337T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215488 | |||||||
chr6:159215614 | A | G | 1 | a0007c0009t0002g0254 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.667+463A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215614 | |||||||
chr6:159215643 | A | G | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.667+492A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215643 | |||||||
chr6:159215776 | T | C | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.667+625T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215776 | |||||||
chr6:159215793 | G | A | 71 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(68): Show |
72 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.667+642G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215793 | |||||||
chr6:159215807 | T | C | 1 | a0016c0054t0003g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.667+656T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215807 | |||||||
chr6:159215840 | T | C | 191 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(188): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.667+689T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215840 | |||||||
chr6:159215875 | G | A | 1 | a0003c0001t0002g0265 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.667+724G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215875 | |||||||
chr6:159215882 | C | T | 1 | a0023c0044t0001g0296 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.667+731C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215882 | |||||||
chr6:159215984 | C | T | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.667+833C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159215984 | |||||||
chr6:159216086 | C | T | 2 | a0009c0013t0002g0029 a0009c0013t0002g0031 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.667+935C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216086 | |||||||
chr6:159216347 | T | C | 4 | a0005c0002t0001g0060 a0005c0002t0001g0132 a0005c0002t0001g0133 others(1): Show |
4 | NA18954.hp1 NA18965.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+1196T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216347 | |||||||
chr6:159216455 | G | A | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.667+1304G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216455 | |||||||
chr6:159216480 | G | A | 3 | a0016c0031t0003g0289 a0016c0054t0003g0037 a0028c0036t0003g0165 |
3 | HG02723.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.667+1329G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216480 | |||||||
chr6:159216489 | C | G | 1 | a0006c0007t0001g0158 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.667+1338C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216489 | |||||||
chr6:159216617 | A | G | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+1466A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216617 | |||||||
chr6:159216623 | C | T | 195 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(192): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.667+1472C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216623 | |||||||
chr6:159216689 | G | A | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.667+1538G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216689 | |||||||
chr6:159216767 | T | C | 9 | a0005c0002t0001g0003 a0005c0002t0001g0027 a0005c0002t0001g0028 others(6): Show |
10 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.667+1616T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216767 | |||||||
chr6:159216859 | G | A | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.667+1708G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216859 | |||||||
chr6:159216991 | T | C | 1 | a0003c0001t0002g0218 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.667+1840T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159216991 | |||||||
chr6:159217094 | T | C | 1 | a0003c0001t0002g0218 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.667+1943T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159217094 | |||||||
chr6:159217147 | G | A | 1 | a0035c0060t0001g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.667+1996G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159217147 | |||||||
chr6:159217189 | T | C | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.667+2038T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159217189 | |||||||
chr6:159217246 | A | G | 66 | a0001c0005t0001g0087 a0003c0001t0002g0006 a0003c0001t0002g0178 others(63): Show |
67 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.667+2095A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159217246 | |||||||
chr6:159217300 | T | C | 1 | a0005c0002t0001g0058 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.667+2149T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159217300 | |||||||
chr6:159217430 | CT | C | 82 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0005c0002t0001g0003 others(79): Show |
84 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.667+2280delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159217430 | |||||||
chr6:159217541 | A | T | 1 | a0018c0047t0002g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.667+2390A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159217541 | |||||||
chr6:159217547 | T | C | 147 | a0001c0005t0006g0137 a0002c0004t0001g0189 a0002c0004t0001g0242 others(144): Show |
150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.667+2396T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159217547 | |||||||
chr6:159217613 | T | C | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+2462T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159217613 | |||||||
chr6:159217652 | G | C | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.667+2501G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159217652 | |||||||
chr6:159218022 | G | T | 2 | a0008c0070t0005g0036 a0026c0041t0002g0155 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.667+2871G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218022 | |||||||
chr6:159218039 | TAG | T | 4 | a0004c0053t0003g0034 a0018c0042t0002g0282 a0018c0047t0002g0163 others(1): Show |
4 | HG03486.hp1 NA19043.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+2891_667+2892d others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr6 | 159218039 | ||||||
chr6:159218163 | C | A | 6 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(3): Show |
6 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.667+3012C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218163 | |||||||
chr6:159218252 | C | T | 76 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0005c0002t0001g0003 others(73): Show |
78 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.667+3101C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218252 | |||||||
chr6:159218312 | G | A | 2 | a0006c0007t0001g0251 a0008c0028t0002g0118 |
2 | NA18954.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.667+3161G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218312 | |||||||
chr6:159218450 | C | T | 126 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(123): Show |
128 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.668-3148C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218450 | |||||||
chr6:159218498 | G | A | 184 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(181): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.668-3100G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218498 | |||||||
chr6:159218540 | G | C | 188 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(185): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.668-3058G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218540 | |||||||
chr6:159218628 | C | G | 193 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(190): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.668-2970C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218628 | |||||||
chr6:159218683 | C | A | 3 | a0016c0031t0003g0289 a0016c0054t0003g0037 a0028c0036t0003g0165 |
3 | HG02723.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.668-2915C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218683 | |||||||
chr6:159218689 | C | A | 3 | a0016c0031t0003g0289 a0016c0054t0003g0037 a0028c0036t0003g0165 |
3 | HG02723.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.668-2909C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218689 | |||||||
chr6:159218753 | C | T | 187 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(184): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.668-2845C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218753 | |||||||
chr6:159218852 | A | G | 192 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(189): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.668-2746A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218852 | |||||||
chr6:159218963 | C | T | 1 | a0005c0002t0001g0138 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.668-2635C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218963 | |||||||
chr6:159218988 | T | C | 2 | a0006c0007t0001g0202 a0006c0007t0001g0258 |
2 | HG02015.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.668-2610T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159218988 | |||||||
chr6:159219041 | C | T | 188 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(185): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.668-2557C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219041 | |||||||
chr6:159219046 | C | CT | 148 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0003c0001t0002g0006 others(145): Show |
150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.668-2540dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr6 | 159219046 | ||||||
chr6:159219046 | C | CTT | 40 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.668-2541_668-2540d others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr6 | 159219046 | ||||||
chr6:159219067 | G | A | 187 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(184): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.668-2531G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219067 | |||||||
chr6:159219143 | A | T | 193 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(190): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.668-2455A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219143 | |||||||
chr6:159219228 | G | T | 2 | a0001c0005t0001g0287 a0001c0010t0003g0286 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.668-2370G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219228 | |||||||
chr6:159219249 | A | C | 188 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(185): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.668-2349A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219249 | |||||||
chr6:159219270 | A | G | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.668-2328A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219270 | |||||||
chr6:159219513 | C | T | 187 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(184): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.668-2085C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219513 | |||||||
chr6:159219533 | C | T | 187 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(184): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.668-2065C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219533 | |||||||
chr6:159219575 | G | A | 1 | a0001c0005t0001g0090 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.668-2023G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219575 | |||||||
chr6:159219626 | A | G | 9 | a0002c0039t0002g0205 a0003c0046t0002g0243 a0009c0013t0002g0025 others(6): Show |
9 | HG01243.hp2 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.668-1972A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219626 | |||||||
chr6:159219677 | T | C | 81 | a0001c0005t0006g0137 a0002c0008t0001g0283 a0004c0069t0001g0007 others(78): Show |
83 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.668-1921T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219677 | |||||||
chr6:159219719 | G | T | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-1879G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219719 | |||||||
chr6:159219869 | G | A | 185 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(182): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.668-1729G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219869 | |||||||
chr6:159219919 | A | T | 6 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-1679A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159219919 | |||||||
chr6:159220041 | A | G | 3 | a0003c0001t0002g0266 a0004c0003t0002g0129 a0004c0019t0001g0096 |
3 | NA18948.hp2 NA18983.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.668-1557A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220041 | |||||||
chr6:159220080 | G | A | 1 | a0032c0075t0002g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.668-1518G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220080 | |||||||
chr6:159220368 | C | T | 65 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(62): Show |
66 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.668-1230C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220368 | |||||||
chr6:159220412 | T | G | 6 | a0005c0002t0001g0064 a0005c0002t0001g0065 a0005c0002t0001g0135 others(3): Show |
6 | HG02155.hp2 NA18947.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.668-1186T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220412 | |||||||
chr6:159220428 | C | T | 185 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(182): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.668-1170C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220428 | |||||||
chr6:159220551 | G | A | 1 | a0005c0002t0001g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.668-1047G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220551 | |||||||
chr6:159220596 | T | A | 1 | a0010c0014t0003g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.668-1002T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220596 | |||||||
chr6:159220648 | T | G | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.668-950T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220648 | |||||||
chr6:159220674 | G | A | 17 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0006t0001g0053 others(14): Show |
17 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.668-924G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220674 | |||||||
chr6:159220706 | G | A | 185 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(182): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.668-892G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220706 | |||||||
chr6:159220795 | C | A | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.668-803C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220795 | |||||||
chr6:159220822 | G | T | 184 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(181): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.668-776G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220822 | |||||||
chr6:159220828 | G | T | 1 | a0015c0030t0003g0033 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.668-770G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220828 | |||||||
chr6:159220829 | T | C | 184 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(181): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.668-769T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220829 | |||||||
chr6:159220973 | C | T | 184 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(181): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.668-625C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159220973 | |||||||
chr6:159221096 | G | A | 184 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(181): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.668-502G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221096 | |||||||
chr6:159221186 | G | A | 6 | a0003c0046t0002g0243 a0009c0013t0002g0025 a0009c0013t0002g0026 others(3): Show |
6 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.668-412G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221186 | |||||||
chr6:159221217 | T | C | 4 | a0009c0032t0003g0288 a0012c0016t0002g0166 a0012c0016t0002g0168 others(1): Show |
4 | HG02976.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-381T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221217 | |||||||
chr6:159221367 | G | A | 1 | a0001c0006t0001g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.668-231G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221367 | |||||||
chr6:159221447 | A | G | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.668-151A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221447 | |||||||
chr6:159221450 | G | A | 6 | a0003c0046t0002g0243 a0009c0013t0002g0025 a0009c0013t0002g0026 others(3): Show |
6 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.668-148G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221450 | |||||||
chr6:159221452 | C | T | 1 | a0002c0018t0004g0175 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.668-146C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221452 | |||||||
chr6:159221465 | G | T | 1 | a0004c0003t0002g0127 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.668-133G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221465 | |||||||
chr6:159221469 | A | G | 186 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(183): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.668-129A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221469 | |||||||
chr6:159221470 | C | G | 1 | a0004c0003t0002g0108 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.668-128C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221470 | |||||||
chr6:159221487 | C | T | 189 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(186): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.668-111C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 5/22 | chr6 | 159221487 | |||||||
chr6:159221745 | C | T | 6 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+49C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159221745 | |||||||
chr6:159221828 | G | A | 178 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(175): Show |
181 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.766+132G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159221828 | |||||||
chr6:159221931 | C | T | 181 | a0003c0001t0002g0006 a0003c0001t0002g0178 a0003c0001t0002g0180 others(178): Show |
184 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.766+235C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159221931 | |||||||
chr6:159222377 | T | C | 1 | a0003c0001t0002g0246 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.766+681T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159222377 | |||||||
chr6:159222381 | T | C | 10 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.766+685T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159222381 | |||||||
chr6:159222406 | C | T | 1 | a0006c0007t0001g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.766+710C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159222406 | |||||||
chr6:159222464 | C | T | 1 | a0001c0005t0001g0087 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.766+768C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159222464 | |||||||
chr6:159222602 | T | C | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.766+906T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159222602 | |||||||
chr6:159222664 | C | A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.767-864C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159222664 | |||||||
chr6:159222726 | G | T | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-802G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159222726 | |||||||
chr6:159222960 | G | A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.767-568G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159222960 | |||||||
chr6:159222984 | A | AT | 9 | a0001c0005t0001g0072 a0001c0005t0001g0090 a0001c0006t0001g0018 others(6): Show |
9 | HG01071.hp2 HG02056.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.767-516dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr6 | 159222984 | ||||||
chr6:159222984 | AT | A | 26 | a0001c0005t0001g0075 a0001c0005t0001g0082 a0001c0005t0001g0106 others(23): Show |
26 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.767-516delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr6 | 159222984 | ||||||
chr6:159222984 | ATTTTTTT others(12): Show |
A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.767-534_767-516del others(19): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr6 | 159222984 | ||||||
chr6:159223012 | T | C | 12 | a0009c0013t0002g0025 a0009c0013t0002g0026 a0009c0013t0002g0029 others(9): Show |
12 | HG01243.hp2 HG02615.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.767-516T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223012 | |||||||
chr6:159223040 | G | T | 1 | a0004c0003t0002g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.767-488G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223040 | |||||||
chr6:159223048 | T | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.767-480T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223048 | |||||||
chr6:159223051 | A | G | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.767-477A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223051 | |||||||
chr6:159223082 | G | A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.767-446G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223082 | |||||||
chr6:159223121 | G | A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.767-407G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223121 | |||||||
chr6:159223157 | A | G | 212 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(209): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.767-371A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223157 | |||||||
chr6:159223166 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.767-362C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223166 | |||||||
chr6:159223187 | G | A | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.767-341G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223187 | |||||||
chr6:159223197 | T | C | 6 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.767-331T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223197 | |||||||
chr6:159223210 | A | G | 1 | a0002c0008t0001g0195 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.767-318A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223210 | |||||||
chr6:159223238 | T | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.767-290T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223238 | |||||||
chr6:159223286 | A | G | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.767-242A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 6/22 | chr6 | 159223286 | |||||||
chr6:159223798 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.884+153C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159223798 | |||||||
chr6:159223811 | G | A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.884+166G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159223811 | |||||||
chr6:159223855 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.884+210C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159223855 | |||||||
chr6:159223900 | G | A | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.884+255G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159223900 | |||||||
chr6:159224346 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.884+701C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159224346 | |||||||
chr6:159224348 | C | T | 4 | a0009c0032t0003g0288 a0012c0016t0002g0166 a0012c0016t0002g0168 others(1): Show |
4 | HG02976.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.884+703C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159224348 | |||||||
chr6:159224458 | C | T | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.884+813C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159224458 | |||||||
chr6:159224530 | A | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.884+885A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159224530 | |||||||
chr6:159224584 | C | T | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.884+939C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159224584 | |||||||
chr6:159224597 | T | C | 1 | a0003c0001t0002g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.885-938T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159224597 | |||||||
chr6:159224723 | C | G | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.885-812C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159224723 | |||||||
chr6:159224751 | A | G | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.885-784A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159224751 | |||||||
chr6:159224819 | A | G | 1 | a0002c0008t0001g0297 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.885-716A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159224819 | |||||||
chr6:159224856 | A | G | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.885-679A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159224856 | |||||||
chr6:159225018 | G | A | 1 | a0003c0043t0002g0197 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.885-517G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159225018 | |||||||
chr6:159225048 | C | T | 12 | a0009c0013t0002g0025 a0009c0013t0002g0026 a0009c0013t0002g0029 others(9): Show |
12 | HG01243.hp2 HG02615.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.885-487C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159225048 | |||||||
chr6:159225049 | G | A | 1 | a0023c0044t0001g0296 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.885-486G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159225049 | |||||||
chr6:159225178 | G | GAC | 86 | a0003c0046t0002g0243 a0005c0002t0001g0003 a0005c0002t0001g0008 others(83): Show |
88 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.885-342_885-341dup others(2): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 159225178 | ||||||
chr6:159225178 | G | GACACACA others(5): Show |
2 | a0005c0002t0001g0058 a0005c0002t0001g0091 |
2 | NA18947.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.885-352_885-341dup others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 159225178 | ||||||
chr6:159225191 | ACACG | A | 74 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(71): Show |
77 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.885-340_885-337del others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 159225191 | ||||||
chr6:159225195 | G | A | 138 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(135): Show |
140 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(137): Show |
intron_variant | MODIFIER | c.885-340G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159225195 | |||||||
chr6:159225200 | G | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.885-335G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159225200 | |||||||
chr6:159225201 | T | A | 1 | a0008c0011t0003g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.885-334T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159225201 | |||||||
chr6:159225202 | C | G | 1 | a0005c0002t0001g0120 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.885-333C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159225202 | |||||||
chr6:159225291 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.885-244C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159225291 | |||||||
chr6:159225301 | T | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.885-234T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159225301 | |||||||
chr6:159225339 | GT | G | 17 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0006t0001g0053 others(14): Show |
17 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.885-189delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 159225339 | ||||||
chr6:159225418 | T | A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.885-117T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 7/22 | chr6 | 159225418 | |||||||
chr6:159225821 | G | A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1072+99G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 8/22 | chr6 | 159225821 | |||||||
chr6:159225877 | C | T | 2 | a0003c0001t0002g0276 a0004c0003t0002g0104 |
2 | HG02148.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1072+155C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 8/22 | chr6 | 159225877 | |||||||
chr6:159225915 | T | A | 1 | a0008c0070t0005g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1072+193T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 8/22 | chr6 | 159225915 | |||||||
chr6:159226021 | G | C | 2 | a0003c0001t0002g0277 a0004c0003t0002g0117 |
2 | NA18969.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1072+299G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 8/22 | chr6 | 159226021 | |||||||
chr6:159226140 | T | C | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073-333T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 8/22 | chr6 | 159226140 | |||||||
chr6:159226380 | T | C | 1 | a0032c0075t0002g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1073-93T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 8/22 | chr6 | 159226380 | |||||||
chr6:159226422 | A | G | 74 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(71): Show |
77 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1073-51A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 8/22 | chr6 | 159226422 | |||||||
chr6:159226720 | A | C | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1180+140A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159226720 | |||||||
chr6:159226897 | G | A | 85 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(82): Show |
87 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.1180+317G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159226897 | |||||||
chr6:159226970 | A | G | 4 | a0004c0069t0001g0007 a0005c0002t0001g0150 a0006c0007t0001g0179 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+390A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159226970 | |||||||
chr6:159227026 | G | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1180+446G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227026 | |||||||
chr6:159227041 | A | T | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1180+461A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227041 | |||||||
chr6:159227063 | G | T | 1 | a0002c0008t0001g0297 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1180+483G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227063 | |||||||
chr6:159227113 | A | G | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1180+533A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227113 | |||||||
chr6:159227122 | A | G | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1180+542A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227122 | |||||||
chr6:159227188 | T | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1180+608T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227188 | |||||||
chr6:159227204 | T | G | 4 | a0009c0032t0003g0288 a0012c0016t0002g0166 a0012c0016t0002g0168 others(1): Show |
4 | HG02976.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+624T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227204 | |||||||
chr6:159227217 | G | A | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180+637G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227217 | |||||||
chr6:159227261 | C | T | 1 | a0001c0006t0001g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1180+681C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227261 | |||||||
chr6:159227297 | G | T | 2 | a0014c0027t0001g0077 a0014c0027t0001g0078 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1180+717G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227297 | |||||||
chr6:159227354 | G | A | 3 | a0001c0005t0001g0015 a0002c0004t0001g0162 a0002c0004t0001g0183 |
3 | HG02055.hp2 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1180+774G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227354 | |||||||
chr6:159227566 | C | T | 1 | a0002c0008t0001g0244 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1180+986C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227566 | |||||||
chr6:159227609 | T | A | 1 | a0022c0056t0001g0124 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1180+1029T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227609 | |||||||
chr6:159227629 | G | A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1180+1049G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227629 | |||||||
chr6:159227646 | C | CT | 11 | a0001c0005t0001g0048 a0001c0005t0001g0051 a0001c0005t0001g0082 others(8): Show |
11 | HG00639.hp2 HG01081.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1180+1081dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr6 | 159227646 | ||||||
chr6:159227646 | CT | C | 50 | a0002c0004t0001g0209 a0005c0002t0001g0014 a0005c0002t0001g0044 others(47): Show |
50 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1180+1081delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr6 | 159227646 | ||||||
chr6:159227646 | CTT | C | 141 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(138): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1180+1080_1180+108 others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr6 | 159227646 | ||||||
chr6:159227648 | T | C | 1 | a0001c0005t0001g0047 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1180+1068T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227648 | |||||||
chr6:159227649 | T | C | 49 | a0005c0002t0001g0014 a0005c0002t0001g0044 a0005c0002t0001g0054 others(46): Show |
49 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1180+1069T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227649 | |||||||
chr6:159227650 | T | C | 141 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(138): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1180+1070T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227650 | |||||||
chr6:159227758 | G | C | 2 | a0008c0011t0003g0052 a0008c0011t0003g0057 |
2 | HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1180+1178G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227758 | |||||||
chr6:159227800 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1180+1220C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227800 | |||||||
chr6:159227831 | A | G | 1 | a0001c0005t0001g0123 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1180+1251A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227831 | |||||||
chr6:159227832 | T | A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1180+1252T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227832 | |||||||
chr6:159227837 | T | A | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1180+1257T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227837 | |||||||
chr6:159227875 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1180+1295C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227875 | |||||||
chr6:159227924 | A | G | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1180+1344A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159227924 | |||||||
chr6:159228006 | C | T | 2 | a0003c0001t0002g0266 a0004c0003t0002g0129 |
2 | NA18983.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1180+1426C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228006 | |||||||
chr6:159228035 | CT | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1180+1464delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr6 | 159228035 | ||||||
chr6:159228037 | T | C | 1 | a0031c0040t0002g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1180+1457T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228037 | |||||||
chr6:159228362 | G | A | 10 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181-1453G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228362 | |||||||
chr6:159228544 | C | CT | 176 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(173): Show |
180 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1181-1271_1181-127 others(5): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228544 | |||||||
chr6:159228545 | G | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1181-1270G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228545 | |||||||
chr6:159228555 | T | A | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1181-1260T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228555 | |||||||
chr6:159228609 | T | C | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1181-1206T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228609 | |||||||
chr6:159228628 | A | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1181-1187A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228628 | |||||||
chr6:159228663 | A | T | 85 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(82): Show |
87 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.1181-1152A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228663 | |||||||
chr6:159228683 | A | C | 1 | a0006c0007t0001g0153 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1181-1132A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228683 | |||||||
chr6:159228713 | A | G | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1181-1102A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228713 | |||||||
chr6:159228715 | T | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1181-1100T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228715 | |||||||
chr6:159228811 | G | T | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1181-1004G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228811 | |||||||
chr6:159228906 | C | A | 1 | a0006c0007t0001g0272 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1181-909C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228906 | |||||||
chr6:159228955 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1181-860C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228955 | |||||||
chr6:159228993 | G | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1181-822G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159228993 | |||||||
chr6:159229096 | T | C | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1181-719T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159229096 | |||||||
chr6:159229142 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1181-673C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159229142 | |||||||
chr6:159229153 | CA | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1181-658delA | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr6 | 159229153 | ||||||
chr6:159229279 | A | G | 1 | a0002c0004t0001g0239 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1181-536A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159229279 | |||||||
chr6:159229294 | C | T | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1181-521C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159229294 | |||||||
chr6:159229581 | G | T | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1181-234G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159229581 | |||||||
chr6:159229621 | C | A | 3 | a0018c0042t0002g0282 a0018c0047t0002g0163 a0032c0075t0002g0298 |
3 | HG03486.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1181-194C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159229621 | |||||||
chr6:159229690 | C | T | 21 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(18): Show |
21 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1181-125C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159229690 | |||||||
chr6:159229735 | G | A | 1 | a0018c0047t0002g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1181-80G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159229735 | |||||||
chr6:159229772 | G | A | 3 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0049t0002g0159 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181-43G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 9/22 | chr6 | 159229772 | |||||||
chr6:159230120 | C | T | 2 | a0003c0001t0002g0006 a0003c0001t0002g0214 |
3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1369+117C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230120 | |||||||
chr6:159230173 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1369+170C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230173 | |||||||
chr6:159230195 | T | G | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1369+192T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230195 | |||||||
chr6:159230215 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1369+212C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230215 | |||||||
chr6:159230247 | A | G | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1369+244A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230247 | |||||||
chr6:159230265 | A | G | 1 | a0018c0042t0002g0282 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1369+262A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230265 | |||||||
chr6:159230271 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1369+268C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230271 | |||||||
chr6:159230292 | G | A | 1 | a0001c0010t0003g0022 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1369+289G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230292 | |||||||
chr6:159230329 | C | G | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1369+326C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230329 | |||||||
chr6:159230515 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1369+512C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230515 | |||||||
chr6:159230639 | T | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1369+636T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230639 | |||||||
chr6:159230693 | C | T | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+690C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230693 | |||||||
chr6:159230694 | A | G | 212 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(209): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1369+691A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230694 | |||||||
chr6:159230742 | T | C | 1 | a0001c0006t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1369+739T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230742 | |||||||
chr6:159230749 | A | G | 21 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0001c0005t0001g0142 others(18): Show |
21 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1369+746A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230749 | |||||||
chr6:159230780 | C | T | 1 | a0032c0075t0002g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1369+777C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230780 | |||||||
chr6:159230837 | C | T | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1369+834C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230837 | |||||||
chr6:159230935 | A | C | 190 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(187): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1369+932A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159230935 | |||||||
chr6:159230954 | G | GTT | 180 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(177): Show |
185 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.1370-921_1370-920d others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 159230954 | ||||||
chr6:159230954 | G | GTTT | 10 | a0003c0001t0002g0216 a0003c0001t0002g0262 a0003c0022t0001g0248 others(7): Show |
10 | HG00408.hp1 HG00438.hp1 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-922_1370-920d others(5): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 159230954 | ||||||
chr6:159231071 | C | A | 107 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1370-811C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159231071 | |||||||
chr6:159231077 | TAAAAATT others(306): Show |
T | 107 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1370-788_1370-476d others(2): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 159231077 | ||||||
chr6:159231097 | C | T | 2 | a0005c0002t0001g0135 a0023c0044t0001g0296 |
2 | HG01109.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1370-785C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159231097 | |||||||
chr6:159231098 | G | A | 12 | a0009c0013t0002g0025 a0009c0013t0002g0026 a0009c0013t0002g0029 others(9): Show |
12 | HG01243.hp2 HG02615.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1370-784G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159231098 | |||||||
chr6:159231326 | G | C | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1370-556G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159231326 | |||||||
chr6:159231365 | G | A | 3 | a0004c0020t0001g0099 a0004c0020t0001g0100 a0004c0020t0001g0107 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1370-517G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159231365 | |||||||
chr6:159231381 | C | CA | 9 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(6): Show |
9 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1370-487dupA | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 159231381 | ||||||
chr6:159231413 | G | A | 107 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1370-469G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159231413 | |||||||
chr6:159231653 | T | G | 1 | a0001c0006t0001g0141 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1370-229T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159231653 | |||||||
chr6:159231808 | A | T | 101 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(98): Show |
104 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1370-74A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159231808 | |||||||
chr6:159231878 | G | A | 3 | a0003c0046t0002g0243 a0015c0030t0003g0032 a0015c0030t0003g0033 |
3 | HG02258.hp2 HG03041.hp1 NA18522.hp1 |
splice_region_variant&intron_variant | LOW | c.1370-4G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 10/22 | chr6 | 159231878 | |||||||
chr6:159234484 | T | C | 14 | a0001c0005t0001g0142 a0001c0006t0001g0053 a0001c0006t0001g0059 others(11): Show |
14 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.3967+5T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159234484 | |||||||
chr6:159234561 | C | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3967+82C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159234561 | |||||||
chr6:159234641 | G | C | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3967+162G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159234641 | |||||||
chr6:159234817 | C | T | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3967+338C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159234817 | |||||||
chr6:159234869 | C | T | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3967+390C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159234869 | |||||||
chr6:159234886 | G | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3967+407G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159234886 | |||||||
chr6:159235006 | C | G | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3967+527C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235006 | |||||||
chr6:159235065 | A | C | 1 | a0001c0062t0001g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3967+586A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235065 | |||||||
chr6:159235075 | G | A | 14 | a0001c0005t0001g0142 a0001c0006t0001g0053 a0001c0006t0001g0059 others(11): Show |
14 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.3967+596G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235075 | |||||||
chr6:159235091 | A | G | 2 | a0014c0027t0001g0077 a0014c0027t0001g0078 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.3967+612A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235091 | |||||||
chr6:159235164 | A | G | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3967+685A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235164 | |||||||
chr6:159235180 | C | T | 1 | a0032c0075t0002g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3967+701C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235180 | |||||||
chr6:159235181 | A | G | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3967+702A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235181 | |||||||
chr6:159235233 | C | T | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3967+754C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235233 | |||||||
chr6:159235269 | C | T | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3967+790C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235269 | |||||||
chr6:159235297 | G | A | 3 | a0016c0031t0003g0289 a0016c0054t0003g0037 a0028c0036t0003g0165 |
3 | HG02723.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3967+818G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235297 | |||||||
chr6:159235317 | AT | A | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3967+850delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr6 | 159235317 | ||||||
chr6:159235555 | C | T | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3968-660C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235555 | |||||||
chr6:159235600 | T | C | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3968-615T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235600 | |||||||
chr6:159235702 | T | G | 22 | a0005c0002t0001g0054 a0005c0002t0001g0060 a0005c0002t0001g0064 others(19): Show |
22 | HG02155.hp2 NA18947.hp1 NA18948.hp1 others(19): Show |
intron_variant | MODIFIER | c.3968-513T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235702 | |||||||
chr6:159235759 | C | T | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3968-456C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235759 | |||||||
chr6:159235866 | A | G | 1 | a0001c0010t0003g0286 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3968-349A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159235866 | |||||||
chr6:159236115 | T | C | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3968-100T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159236115 | |||||||
chr6:159236163 | G | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3968-52G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 11/22 | chr6 | 159236163 | |||||||
chr6:159236543 | C | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4068+228C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159236543 | |||||||
chr6:159236555 | G | A | 74 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(71): Show |
77 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.4068+240G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159236555 | |||||||
chr6:159236562 | C | T | 1 | a0006c0007t0001g0247 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4068+247C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159236562 | |||||||
chr6:159236822 | C | T | 1 | a0001c0010t0003g0074 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4068+507C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159236822 | |||||||
chr6:159236886 | T | A | 1 | a0005c0002t0001g0145 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4068+571T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159236886 | |||||||
chr6:159236996 | A | G | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4068+681A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159236996 | |||||||
chr6:159236997 | C | G | 25 | a0001c0005t0001g0142 a0001c0006t0001g0053 a0001c0006t0001g0059 others(22): Show |
25 | HG00140.hp1 HG00639.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.4068+682C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159236997 | |||||||
chr6:159237010 | C | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4068+695C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159237010 | |||||||
chr6:159237095 | C | G | 7 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4068+780C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159237095 | |||||||
chr6:159237151 | G | A | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4068+836G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159237151 | |||||||
chr6:159237385 | T | C | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4068+1070T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159237385 | |||||||
chr6:159237401 | G | A | 1 | a0001c0006t0001g0020 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4068+1086G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159237401 | |||||||
chr6:159237427 | C | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4068+1112C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159237427 | |||||||
chr6:159237661 | A | T | 1 | a0003c0001t0002g0156 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.4069-893A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159237661 | |||||||
chr6:159237694 | A | G | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4069-860A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159237694 | |||||||
chr6:159237820 | C | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4069-734C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159237820 | |||||||
chr6:159237875 | G | A | 94 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(91): Show |
96 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.4069-679G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159237875 | |||||||
chr6:159238023 | T | C | 1 | a0009c0013t0002g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4069-531T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238023 | |||||||
chr6:159238097 | CTT | C | 74 | a0002c0008t0001g0231 a0003c0001t0002g0006 a0003c0001t0002g0156 others(71): Show |
77 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.4069-440_4069-439d others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 159238097 | ||||||
chr6:159238097 | CTTT | C | 127 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(124): Show |
129 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.4069-441_4069-439d others(5): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 159238097 | ||||||
chr6:159238097 | CTTTT | C | 7 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4069-442_4069-439d others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 159238097 | ||||||
chr6:159238139 | A | C | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4069-415A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238139 | |||||||
chr6:159238151 | G | T | 6 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4069-403G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238151 | |||||||
chr6:159238157 | G | C | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4069-397G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238157 | |||||||
chr6:159238178 | G | A | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4069-376G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238178 | |||||||
chr6:159238184 | G | A | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4069-370G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238184 | |||||||
chr6:159238199 | G | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4069-355G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238199 | |||||||
chr6:159238331 | C | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4069-223C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238331 | |||||||
chr6:159238376 | C | T | 1 | a0001c0006t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4069-178C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238376 | |||||||
chr6:159238449 | C | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4069-105C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238449 | |||||||
chr6:159238491 | A | G | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4069-63A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 12/22 | chr6 | 159238491 | |||||||
chr6:159238764 | A | G | 1 | a0003c0001t0002g0246 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4180+99A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159238764 | |||||||
chr6:159238787 | G | A | 2 | a0012c0016t0002g0166 a0012c0016t0002g0168 |
2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4180+122G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159238787 | |||||||
chr6:159238817 | C | G | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4180+152C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159238817 | |||||||
chr6:159238880 | G | A | 1 | a0008c0028t0002g0055 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4180+215G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159238880 | |||||||
chr6:159238904 | G | A | 1 | a0004c0053t0003g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4180+239G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159238904 | |||||||
chr6:159238939 | G | A | 10 | a0001c0006t0001g0053 a0001c0006t0001g0059 a0001c0010t0003g0013 others(7): Show |
10 | HG00140.hp1 HG00639.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4180+274G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159238939 | |||||||
chr6:159238979 | G | A | 1 | a0001c0006t0001g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4180+314G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159238979 | |||||||
chr6:159239033 | G | A | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4180+368G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159239033 | |||||||
chr6:159239073 | C | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4180+408C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159239073 | |||||||
chr6:159239095 | A | T | 2 | a0005c0002t0001g0066 a0005c0002t0001g0119 |
2 | HG02155.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.4181-422A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159239095 | |||||||
chr6:159239116 | C | T | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4181-401C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159239116 | |||||||
chr6:159239223 | T | C | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4181-294T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159239223 | |||||||
chr6:159239474 | T | A | 7 | a0009c0032t0003g0288 a0012c0016t0002g0166 a0012c0016t0002g0168 others(4): Show |
7 | HG02723.hp1 HG02886.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.4181-43T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 13/22 | chr6 | 159239474 | |||||||
chr6:159239992 | A | G | 3 | a0005c0002t0001g0066 a0005c0002t0001g0119 a0006c0007t0001g0247 |
3 | HG02135.hp2 HG02155.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.4621+35A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159239992 | |||||||
chr6:159240008 | C | T | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4621+51C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159240008 | |||||||
chr6:159240144 | G | A | 2 | a0029c0058t0001g0080 a0034c0038t0002g0152 |
2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.4621+187G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159240144 | |||||||
chr6:159240178 | GA | G | 209 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(206): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.4621+228delA | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr6 | 159240178 | ||||||
chr6:159240185 | A | C | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4621+228A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159240185 | |||||||
chr6:159240638 | C | T | 92 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(89): Show |
94 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.4621+681C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159240638 | |||||||
chr6:159241032 | G | A | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4621+1075G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159241032 | |||||||
chr6:159241104 | G | A | 74 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(71): Show |
77 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.4621+1147G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159241104 | |||||||
chr6:159241270 | T | C | 1 | a0006c0007t0001g0161 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4621+1313T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159241270 | |||||||
chr6:159241276 | G | A | 7 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4621+1319G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159241276 | |||||||
chr6:159241315 | C | T | 7 | a0005c0002t0001g0064 a0005c0002t0001g0065 a0005c0002t0001g0135 others(4): Show |
7 | HG02155.hp2 NA18947.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.4621+1358C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159241315 | |||||||
chr6:159241467 | A | G | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4621+1510A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159241467 | |||||||
chr6:159241493 | G | A | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4621+1536G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159241493 | |||||||
chr6:159241575 | T | C | 1 | a0005c0002t0001g0132 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.4621+1618T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159241575 | |||||||
chr6:159241606 | A | G | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.4621+1649A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159241606 | |||||||
chr6:159241784 | G | A | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4621+1827G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159241784 | |||||||
chr6:159242013 | A | G | 1 | a0008c0011t0003g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4621+2056A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242013 | |||||||
chr6:159242017 | C | G | 1 | a0004c0003t0002g0042 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4621+2060C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242017 | |||||||
chr6:159242022 | A | T | 1 | a0018c0042t0002g0282 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4621+2065A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242022 | |||||||
chr6:159242090 | C | T | 17 | a0005c0002t0001g0008 a0006c0026t0001g0252 a0006c0026t0001g0253 others(14): Show |
18 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.4621+2133C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242090 | |||||||
chr6:159242249 | G | A | 1 | a0010c0014t0003g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.4621+2292G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242249 | |||||||
chr6:159242322 | G | A | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4621+2365G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242322 | |||||||
chr6:159242382 | C | T | 5 | a0005c0002t0001g0121 a0005c0002t0001g0122 a0006c0007t0001g0202 others(2): Show |
5 | HG02015.hp1 HG02523.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.4621+2425C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242382 | |||||||
chr6:159242517 | T | A | 73 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(70): Show |
76 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.4621+2560T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242517 | |||||||
chr6:159242671 | C | T | 12 | a0001c0005t0001g0142 a0001c0006t0001g0053 a0001c0006t0001g0059 others(9): Show |
12 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.4621+2714C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242671 | |||||||
chr6:159242689 | G | A | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4621+2732G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242689 | |||||||
chr6:159242718 | G | A | 1 | a0017c0025t0001g0200 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.4621+2761G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242718 | |||||||
chr6:159242799 | C | G | 12 | a0001c0005t0001g0142 a0001c0006t0001g0053 a0001c0006t0001g0059 others(9): Show |
12 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.4621+2842C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242799 | |||||||
chr6:159242845 | T | G | 1 | a0005c0002t0001g0138 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4621+2888T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242845 | |||||||
chr6:159242949 | C | T | 6 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4621+2992C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159242949 | |||||||
chr6:159243171 | CT | C | 207 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(204): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.4621+3225delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr6 | 159243171 | ||||||
chr6:159243189 | C | T | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4621+3232C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159243189 | |||||||
chr6:159243290 | G | T | 92 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(89): Show |
94 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.4621+3333G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159243290 | |||||||
chr6:159243484 | G | T | 209 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(206): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.4622-3417G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159243484 | |||||||
chr6:159243485 | T | A | 1 | a0001c0055t0003g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4622-3416T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159243485 | |||||||
chr6:159243664 | T | C | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4622-3237T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159243664 | |||||||
chr6:159243739 | T | A | 4 | a0001c0005t0001g0048 a0001c0005t0006g0137 a0001c0062t0001g0083 others(1): Show |
4 | NA18968.hp2 NA19011.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.4622-3162T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159243739 | |||||||
chr6:159243884 | G | C | 1 | a0002c0004t0007g0208 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4622-3017G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159243884 | |||||||
chr6:159244021 | G | T | 1 | a0002c0004t0001g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4622-2880G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244021 | |||||||
chr6:159244051 | G | A | 3 | a0003c0046t0002g0243 a0015c0030t0003g0032 a0015c0030t0003g0033 |
3 | HG02258.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4622-2850G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244051 | |||||||
chr6:159244104 | T | G | 1 | a0002c0008t0001g0245 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4622-2797T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244104 | |||||||
chr6:159244114 | T | C | 1 | a0002c0008t0001g0224 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4622-2787T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244114 | |||||||
chr6:159244146 | C | T | 4 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(1): Show |
4 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4622-2755C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244146 | |||||||
chr6:159244366 | T | C | 2 | a0002c0004t0001g0164 a0002c0004t0001g0228 |
2 | HG01256.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.4622-2535T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244366 | |||||||
chr6:159244534 | G | A | 1 | a0004c0003t0002g0130 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4622-2367G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244534 | |||||||
chr6:159244580 | G | A | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4622-2321G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244580 | |||||||
chr6:159244645 | A | T | 6 | a0003c0012t0004g0171 a0003c0012t0004g0185 a0003c0012t0004g0186 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4622-2256A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244645 | |||||||
chr6:159244660 | G | T | 213 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(210): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.4622-2241G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244660 | |||||||
chr6:159244730 | G | A | 1 | a0001c0006t0001g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4622-2171G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244730 | |||||||
chr6:159244897 | A | G | 6 | a0005c0002t0001g0060 a0005c0002t0001g0132 a0005c0002t0001g0134 others(3): Show |
6 | NA18954.hp2 NA18965.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.4622-2004A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244897 | |||||||
chr6:159244914 | T | A | 213 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(210): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.4622-1987T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244914 | |||||||
chr6:159244966 | G | T | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4622-1935G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159244966 | |||||||
chr6:159245004 | A | G | 213 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(210): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.4622-1897A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159245004 | |||||||
chr6:159245053 | C | T | 2 | a0004c0069t0001g0007 a0023c0044t0001g0296 |
2 | HG01109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4622-1848C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159245053 | |||||||
chr6:159245065 | A | G | 1 | a0001c0006t0001g0146 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.4622-1836A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159245065 | |||||||
chr6:159245078 | G | A | 1 | a0007c0009t0002g0257 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4622-1823G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159245078 | |||||||
chr6:159245432 | T | C | 4 | a0009c0013t0002g0025 a0009c0013t0002g0026 a0009c0013t0002g0029 others(1): Show |
4 | HG01243.hp2 HG02615.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4622-1469T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159245432 | |||||||
chr6:159245452 | C | T | 6 | a0001c0005t0001g0142 a0001c0010t0003g0286 a0003c0046t0002g0243 others(3): Show |
6 | HG01934.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4622-1449C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159245452 | |||||||
chr6:159245680 | C | T | 1 | a0004c0003t0002g0127 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4622-1221C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159245680 | |||||||
chr6:159245713 | C | A | 1 | a0001c0006t0001g0146 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.4622-1188C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159245713 | |||||||
chr6:159245729 | AGTCATTA others(316): Show |
A | 214 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(211): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.4622-1154_4622-832 others(3): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr6 | 159245729 | ||||||
chr6:159245742 | A | AT | 19 | a0005c0002t0001g0003 a0005c0002t0001g0027 a0005c0002t0001g0028 others(16): Show |
20 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.4622-1135dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr6 | 159245742 | ||||||
chr6:159245742 | AT | A | 6 | a0005c0002t0001g0064 a0005c0002t0001g0065 a0005c0002t0001g0135 others(3): Show |
6 | HG02155.hp2 HG03710.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.4622-1135delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr6 | 159245742 | ||||||
chr6:159245772 | G | A | 2 | a0005c0002t0001g0150 a0006c0007t0001g0179 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4622-1129G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159245772 | |||||||
chr6:159246000 | C | T | 1 | a0013c0024t0001g0190 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4622-901C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159246000 | |||||||
chr6:159246195 | G | A | 214 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(211): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.4622-706G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159246195 | |||||||
chr6:159246305 | A | G | 214 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(211): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.4622-596A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159246305 | |||||||
chr6:159246572 | G | A | 1 | a0005c0002t0001g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4622-329G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159246572 | |||||||
chr6:159246646 | G | A | 1 | a0002c0004t0001g0210 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4622-255G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159246646 | |||||||
chr6:159246840 | T | C | 1 | a0003c0001t0002g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4622-61T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159246840 | |||||||
chr6:159246848 | G | A | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4622-53G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 14/22 | chr6 | 159246848 | |||||||
chr6:159247054 | G | A | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4690+85G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247054 | |||||||
chr6:159247094 | C | T | 1 | a0032c0075t0002g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4690+125C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247094 | |||||||
chr6:159247130 | G | A | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4690+161G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247130 | |||||||
chr6:159247222 | C | T | 4 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4690+253C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247222 | |||||||
chr6:159247440 | G | A | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4690+471G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247440 | |||||||
chr6:159247467 | G | T | 4 | a0005c0002t0001g0133 a0006c0007t0001g0157 a0006c0007t0001g0158 others(1): Show |
4 | NA18948.hp1 NA18954.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.4690+498G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247467 | |||||||
chr6:159247481 | G | C | 1 | a0008c0070t0005g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4690+512G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247481 | |||||||
chr6:159247594 | A | T | 66 | a0003c0001t0002g0226 a0005c0002t0001g0003 a0005c0002t0001g0008 others(63): Show |
67 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.4690+625A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247594 | |||||||
chr6:159247604 | C | T | 96 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(93): Show |
97 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.4690+635C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247604 | |||||||
chr6:159247630 | G | T | 263 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(260): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.4690+661G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247630 | |||||||
chr6:159247698 | C | CA | 67 | a0003c0001t0002g0226 a0005c0002t0001g0003 a0005c0002t0001g0008 others(64): Show |
68 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.4690+730dupA | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 159247698 | ||||||
chr6:159247742 | CA | C | 66 | a0003c0001t0002g0226 a0005c0002t0001g0003 a0005c0002t0001g0008 others(63): Show |
67 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.4690+781delA | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 159247742 | ||||||
chr6:159247825 | A | G | 1 | a0001c0057t0002g0024 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4690+856A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247825 | |||||||
chr6:159247996 | C | T | 4 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4690+1027C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159247996 | |||||||
chr6:159248040 | T | C | 1 | a0001c0005t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4691-999T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248040 | |||||||
chr6:159248216 | T | C | 5 | a0002c0004t0001g0189 a0002c0004t0001g0242 a0003c0022t0002g0217 others(2): Show |
5 | HG02056.hp1 NA18956.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4691-823T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248216 | |||||||
chr6:159248269 | C | T | 66 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(63): Show |
67 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.4691-770C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248269 | |||||||
chr6:159248272 | C | G | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4691-767C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248272 | |||||||
chr6:159248311 | AT | A | 65 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(62): Show |
66 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.4691-715delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 159248311 | ||||||
chr6:159248360 | C | T | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4691-679C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248360 | |||||||
chr6:159248367 | G | A | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4691-672G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248367 | |||||||
chr6:159248494 | C | G | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4691-545C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248494 | |||||||
chr6:159248494 | C | T | 1 | a0006c0007t0001g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4691-545C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248494 | |||||||
chr6:159248612 | A | T | 66 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(63): Show |
67 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.4691-427A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248612 | |||||||
chr6:159248794 | C | G | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4691-245C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248794 | |||||||
chr6:159248859 | G | A | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4691-180G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248859 | |||||||
chr6:159248917 | G | GTGTC | 67 | a0001c0006t0001g0147 a0002c0008t0001g0230 a0005c0002t0001g0003 others(64): Show |
68 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.4691-119_4691-118i others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 159248917 | ||||||
chr6:159248921 | G | C | 255 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(252): Show |
261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.4691-118G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159248921 | |||||||
chr6:159248921 | G | GTC | 7 | a0002c0018t0004g0175 a0003c0012t0004g0171 a0003c0012t0004g0185 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4691-117_4691-116i others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 159248921 | ||||||
chr6:159249022 | C | G | 1 | a0012c0037t0002g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4691-17C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 15/22 | chr6 | 159249022 | |||||||
chr6:159249244 | A | G | 279 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(276): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.4834+62A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159249244 | |||||||
chr6:159249271 | G | A | 96 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(93): Show |
97 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.4834+89G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159249271 | |||||||
chr6:159249404 | A | T | 2 | a0002c0004t0001g0172 a0002c0004t0001g0176 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4834+222A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159249404 | |||||||
chr6:159249535 | G | A | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.4834+353G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159249535 | |||||||
chr6:159249781 | A | T | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4834+599A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159249781 | |||||||
chr6:159249946 | G | A | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.4834+764G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159249946 | |||||||
chr6:159250060 | C | T | 96 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(93): Show |
97 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.4834+878C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159250060 | |||||||
chr6:159250236 | A | G | 8 | a0001c0010t0003g0013 a0001c0010t0003g0022 a0001c0010t0003g0043 others(5): Show |
8 | HG00140.hp1 HG00639.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.4834+1054A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159250236 | |||||||
chr6:159250252 | T | A | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.4835-1050T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159250252 | |||||||
chr6:159250376 | A | G | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.4835-926A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159250376 | |||||||
chr6:159250604 | T | C | 263 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(260): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.4835-698T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159250604 | |||||||
chr6:159250672 | A | G | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4835-630A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159250672 | |||||||
chr6:159250675 | A | G | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.4835-627A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159250675 | |||||||
chr6:159250693 | A | T | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.4835-609A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159250693 | |||||||
chr6:159250734 | C | G | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4835-568C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159250734 | |||||||
chr6:159250974 | A | G | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4835-328A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159250974 | |||||||
chr6:159251066 | A | T | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4835-236A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159251066 | |||||||
chr6:159251217 | G | C | 1 | a0003c0022t0001g0248 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4835-85G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159251217 | |||||||
chr6:159251272 | A | G | 7 | a0002c0018t0004g0175 a0003c0012t0004g0171 a0003c0012t0004g0185 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4835-30A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159251272 | |||||||
chr6:159251277 | A | G | 3 | a0003c0012t0004g0171 a0005c0002t0001g0089 a0006c0007t0001g0201 |
3 | HG02895.hp2 NA18956.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.4835-25A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 16/22 | chr6 | 159251277 | |||||||
chr6:159251623 | A | G | 1 | a0008c0070t0005g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5065+91A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159251623 | |||||||
chr6:159251766 | C | T | 1 | a0003c0001t0002g0213 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5065+234C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159251766 | |||||||
chr6:159251769 | G | A | 6 | a0002c0039t0002g0205 a0003c0001t0002g0215 a0009c0013t0002g0025 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.5065+237G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159251769 | |||||||
chr6:159251815 | T | C | 1 | a0005c0002t0001g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5065+283T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159251815 | |||||||
chr6:159251905 | C | A | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.5065+373C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159251905 | |||||||
chr6:159251928 | G | A | 3 | a0001c0063t0002g0285 a0003c0046t0002g0243 a0004c0053t0003g0034 |
3 | HG03540.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5065+396G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159251928 | |||||||
chr6:159251930 | G | A | 1 | a0004c0019t0001g0063 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.5065+398G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159251930 | |||||||
chr6:159251944 | G | A | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5065+412G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159251944 | |||||||
chr6:159251953 | C | G | 1 | a0005c0015t0001g0291 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5065+421C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159251953 | |||||||
chr6:159251957 | T | G | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.5065+425T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159251957 | |||||||
chr6:159252054 | A | G | 1 | a0001c0006t0001g0088 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.5065+522A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252054 | |||||||
chr6:159252099 | T | C | 2 | a0001c0005t0001g0073 a0002c0004t0001g0196 |
2 | NA18983.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.5065+567T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252099 | |||||||
chr6:159252126 | T | C | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.5065+594T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252126 | |||||||
chr6:159252214 | A | G | 263 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(260): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.5065+682A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252214 | |||||||
chr6:159252221 | AT | A | 6 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(3): Show |
6 | HG01243.hp2 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.5065+697delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr6 | 159252221 | ||||||
chr6:159252393 | C | T | 65 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(62): Show |
66 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.5065+861C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252393 | |||||||
chr6:159252407 | T | C | 4 | a0001c0010t0003g0286 a0016c0031t0003g0289 a0016c0054t0003g0037 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.5065+875T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252407 | |||||||
chr6:159252409 | A | G | 3 | a0004c0020t0001g0099 a0004c0020t0001g0100 a0004c0020t0001g0107 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5065+877A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252409 | |||||||
chr6:159252576 | C | T | 77 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(74): Show |
81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.5065+1044C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252576 | |||||||
chr6:159252623 | G | A | 4 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5065+1091G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252623 | |||||||
chr6:159252627 | C | T | 1 | a0006c0007t0001g0251 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.5065+1095C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252627 | |||||||
chr6:159252889 | T | C | 1 | a0004c0003t0002g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5065+1357T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252889 | |||||||
chr6:159252927 | C | T | 166 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(163): Show |
168 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.5065+1395C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252927 | |||||||
chr6:159252986 | T | C | 166 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(163): Show |
168 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.5065+1454T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159252986 | |||||||
chr6:159253145 | A | C | 4 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5065+1613A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159253145 | |||||||
chr6:159253301 | A | G | 1 | a0005c0002t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5065+1769A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159253301 | |||||||
chr6:159253378 | G | A | 5 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5065+1846G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159253378 | |||||||
chr6:159253754 | G | A | 4 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5065+2222G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159253754 | |||||||
chr6:159253776 | G | A | 3 | a0004c0003t0002g0101 a0004c0003t0002g0108 a0004c0003t0002g0109 |
3 | HG00408.hp1 NA19063.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.5065+2244G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159253776 | |||||||
chr6:159253869 | C | T | 1 | a0006c0007t0001g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5065+2337C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159253869 | |||||||
chr6:159253872 | T | C | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.5065+2340T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159253872 | |||||||
chr6:159253887 | C | T | 1 | a0004c0003t0002g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5065+2355C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159253887 | |||||||
chr6:159253907 | C | G | 1 | a0008c0011t0003g0052 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5065+2375C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159253907 | |||||||
chr6:159253970 | A | C | 1 | a0001c0010t0003g0022 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5065+2438A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159253970 | |||||||
chr6:159254041 | A | G | 1 | a0012c0037t0002g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5066-2482A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254041 | |||||||
chr6:159254091 | C | T | 1 | a0008c0028t0002g0055 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5066-2432C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254091 | |||||||
chr6:159254252 | T | C | 5 | a0001c0010t0003g0286 a0001c0055t0003g0062 a0016c0031t0003g0289 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5066-2271T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254252 | |||||||
chr6:159254349 | A | C | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.5066-2174A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254349 | |||||||
chr6:159254671 | G | A | 1 | a0001c0006t0001g0004 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5066-1852G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254671 | |||||||
chr6:159254700 | T | G | 4 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5066-1823T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254700 | |||||||
chr6:159254707 | CA | C | 30 | a0001c0005t0001g0072 a0001c0006t0001g0020 a0001c0006t0001g0146 others(27): Show |
30 | HG00735.hp2 HG00741.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.5066-1793delA | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr6 | 159254707 | ||||||
chr6:159254707 | CAA | C | 220 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(217): Show |
225 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.5066-1794_5066-179 others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr6 | 159254707 | ||||||
chr6:159254707 | CAAA | C | 21 | a0001c0005t0001g0051 a0001c0005t0001g0106 a0001c0006t0001g0018 others(18): Show |
22 | HG01074.hp1 HG01256.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5066-1795_5066-179 others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr6 | 159254707 | ||||||
chr6:159254740 | T | C | 166 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(163): Show |
168 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.5066-1783T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254740 | |||||||
chr6:159254779 | G | A | 166 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(163): Show |
168 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.5066-1744G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254779 | |||||||
chr6:159254842 | T | G | 2 | a0001c0006t0001g0088 a0002c0008t0001g0231 |
2 | NA18980.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.5066-1681T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254842 | |||||||
chr6:159254862 | C | T | 1 | a0001c0005t0001g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5066-1661C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254862 | |||||||
chr6:159254973 | T | C | 1 | a0005c0015t0001g0292 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5066-1550T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159254973 | |||||||
chr6:159255012 | A | G | 1 | a0002c0008t0001g0244 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.5066-1511A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159255012 | |||||||
chr6:159255108 | G | A | 1 | a0005c0002t0001g0089 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.5066-1415G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159255108 | |||||||
chr6:159255173 | G | C | 1 | a0002c0004t0001g0209 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.5066-1350G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159255173 | |||||||
chr6:159255214 | G | T | 1 | a0001c0006t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5066-1309G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159255214 | |||||||
chr6:159255417 | C | T | 5 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5066-1106C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159255417 | |||||||
chr6:159255510 | C | T | 52 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(49): Show |
52 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.5066-1013C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159255510 | |||||||
chr6:159255513 | C | A | 166 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(163): Show |
168 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.5066-1010C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159255513 | |||||||
chr6:159255747 | A | G | 2 | a0004c0003t0002g0103 a0004c0003t0002g0110 |
2 | HG03239.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.5066-776A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159255747 | |||||||
chr6:159256157 | C | T | 1 | a0005c0015t0001g0291 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5066-366C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159256157 | |||||||
chr6:159256186 | G | T | 1 | a0005c0002t0001g0119 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.5066-337G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159256186 | |||||||
chr6:159256388 | G | A | 2 | a0001c0010t0003g0013 a0001c0010t0003g0022 |
2 | HG03927.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.5066-135G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159256388 | |||||||
chr6:159256389 | C | T | 1 | a0034c0038t0002g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5066-134C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159256389 | |||||||
chr6:159256441 | C | A | 1 | a0006c0007t0001g0194 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.5066-82C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159256441 | |||||||
chr6:159256466 | C | T | 166 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(163): Show |
168 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.5066-57C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 17/22 | chr6 | 159256466 | |||||||
chr6:159256697 | G | C | 1 | a0003c0001t0002g0246 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5174+66G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159256697 | |||||||
chr6:159256748 | T | C | 2 | a0001c0006t0001g0088 a0002c0008t0001g0231 |
2 | NA18980.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.5174+117T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159256748 | |||||||
chr6:159256808 | G | A | 166 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(163): Show |
168 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.5174+177G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159256808 | |||||||
chr6:159256921 | C | G | 77 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(74): Show |
81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.5174+290C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159256921 | |||||||
chr6:159256960 | A | G | 171 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(168): Show |
173 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.5174+329A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159256960 | |||||||
chr6:159257104 | T | G | 77 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(74): Show |
81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.5174+473T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159257104 | |||||||
chr6:159257249 | G | A | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5174+618G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159257249 | |||||||
chr6:159257411 | T | A | 65 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(62): Show |
66 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.5174+780T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159257411 | |||||||
chr6:159257419 | C | T | 1 | a0012c0037t0002g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5174+788C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159257419 | |||||||
chr6:159257567 | G | C | 101 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(98): Show |
102 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.5174+936G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159257567 | |||||||
chr6:159257659 | C | T | 6 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(3): Show |
6 | HG00741.hp1 HG01243.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.5174+1028C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159257659 | |||||||
chr6:159257680 | G | A | 1 | a0007c0009t0002g0274 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5174+1049G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159257680 | |||||||
chr6:159257772 | A | G | 1 | a0004c0003t0002g0127 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5174+1141A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159257772 | |||||||
chr6:159257802 | A | C | 166 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(163): Show |
168 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.5174+1171A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159257802 | |||||||
chr6:159257894 | G | T | 1 | a0003c0001t0002g0277 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.5174+1263G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159257894 | |||||||
chr6:159257905 | C | CT | 94 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(91): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.5174+1292dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr6 | 159257905 | ||||||
chr6:159257905 | CTT | C | 69 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(66): Show |
70 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.5174+1291_5174+129 others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr6 | 159257905 | ||||||
chr6:159257905 | CTTT | C | 95 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(92): Show |
96 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.5174+1290_5174+129 others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr6 | 159257905 | ||||||
chr6:159258007 | C | T | 1 | a0002c0004t0001g0193 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5174+1376C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159258007 | |||||||
chr6:159258266 | G | A | 1 | a0012c0016t0002g0181 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5174+1635G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159258266 | |||||||
chr6:159258308 | A | G | 65 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(62): Show |
66 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.5174+1677A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159258308 | |||||||
chr6:159258331 | G | GGTGTACA others(5): Show |
1 | a0006c0007t0001g0161 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5174+1701_5174+171 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr6 | 159258331 | ||||||
chr6:159258377 | G | A | 7 | a0002c0018t0004g0175 a0003c0012t0004g0171 a0003c0012t0004g0185 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.5174+1746G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159258377 | |||||||
chr6:159258397 | T | C | 7 | a0002c0018t0004g0175 a0003c0012t0004g0171 a0003c0012t0004g0185 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.5174+1766T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159258397 | |||||||
chr6:159258660 | T | A | 1 | a0003c0022t0002g0217 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.5174+2029T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159258660 | |||||||
chr6:159259193 | T | C | 65 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(62): Show |
66 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.5175-1997T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159259193 | |||||||
chr6:159259194 | A | G | 2 | a0005c0002t0001g0133 a0006c0007t0001g0157 |
2 | NA18954.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.5175-1996A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159259194 | |||||||
chr6:159259207 | A | G | 7 | a0002c0018t0004g0175 a0003c0012t0004g0171 a0003c0012t0004g0185 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.5175-1983A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159259207 | |||||||
chr6:159259489 | C | T | 5 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5175-1701C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159259489 | |||||||
chr6:159259643 | A | C | 1 | a0012c0037t0002g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5175-1547A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159259643 | |||||||
chr6:159259712 | T | C | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5175-1478T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159259712 | |||||||
chr6:159259748 | G | A | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5175-1442G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159259748 | |||||||
chr6:159259961 | C | T | 65 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(62): Show |
66 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.5175-1229C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159259961 | |||||||
chr6:159260020 | T | C | 100 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(97): Show |
101 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.5175-1170T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260020 | |||||||
chr6:159260139 | G | T | 5 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5175-1051G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260139 | |||||||
chr6:159260358 | C | G | 208 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(205): Show |
210 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.5175-832C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260358 | |||||||
chr6:159260440 | A | C | 65 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(62): Show |
66 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.5175-750A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260440 | |||||||
chr6:159260449 | C | T | 3 | a0001c0005t0001g0075 a0001c0005t0001g0106 a0002c0004t0001g0239 |
3 | HG01074.hp1 HG02735.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.5175-741C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260449 | |||||||
chr6:159260459 | A | C | 1 | a0005c0002t0001g0003 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.5175-731A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260459 | |||||||
chr6:159260522 | G | A | 2 | a0003c0001t0002g0188 a0004c0003t0002g0068 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.5175-668G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260522 | |||||||
chr6:159260820 | G | A | 1 | a0004c0069t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5175-370G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260820 | |||||||
chr6:159260841 | A | G | 1 | a0003c0001t0002g0260 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.5175-349A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260841 | |||||||
chr6:159260867 | A | T | 78 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(75): Show |
82 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.5175-323A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260867 | |||||||
chr6:159260918 | C | T | 1 | a0005c0002t0001g0060 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.5175-272C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159260918 | |||||||
chr6:159261166 | A | G | 5 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(2): Show |
5 | HG02109.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.5175-24A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159261166 | |||||||
chr6:159261174 | C | T | 172 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(169): Show |
174 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.5175-16C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 18/22 | chr6 | 159261174 | |||||||
chr6:159261359 | T | C | 1 | a0005c0002t0001g0027 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5254+90T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159261359 | |||||||
chr6:159261426 | A | G | 4 | a0001c0005t0001g0082 a0001c0005t0001g0123 a0002c0004t0001g0221 others(1): Show |
4 | HG00639.hp2 HG01081.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.5254+157A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159261426 | |||||||
chr6:159261435 | C | T | 2 | a0005c0002t0001g0089 a0006c0007t0001g0201 |
2 | NA18956.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.5254+166C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159261435 | |||||||
chr6:159261502 | A | C | 1 | a0013c0024t0001g0190 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5254+233A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159261502 | |||||||
chr6:159261742 | C | T | 75 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(72): Show |
79 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.5254+473C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159261742 | |||||||
chr6:159261753 | A | G | 2 | a0002c0021t0001g0169 a0002c0021t0001g0170 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5254+484A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159261753 | |||||||
chr6:159261948 | A | AT | 99 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(96): Show |
100 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.5254+687dupT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 159261948 | ||||||
chr6:159261948 | A | T | 3 | a0005c0002t0001g0038 a0005c0002t0001g0039 a0005c0015t0001g0290 |
3 | HG01891.hp1 HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.5254+679A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159261948 | |||||||
chr6:159262203 | C | G | 1 | a0007c0009t0003g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5254+934C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159262203 | |||||||
chr6:159262825 | C | T | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5254+1556C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159262825 | |||||||
chr6:159262844 | G | T | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5254+1575G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159262844 | |||||||
chr6:159262969 | C | T | 1 | a0011c0023t0002g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5254+1700C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159262969 | |||||||
chr6:159263050 | C | T | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5254+1781C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263050 | |||||||
chr6:159263054 | G | C | 7 | a0002c0018t0004g0175 a0003c0012t0004g0171 a0003c0012t0004g0185 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.5254+1785G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263054 | |||||||
chr6:159263093 | C | T | 1 | a0002c0008t0001g0231 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5254+1824C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263093 | |||||||
chr6:159263127 | C | T | 1 | a0026c0041t0002g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5255-1848C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263127 | |||||||
chr6:159263358 | G | A | 63 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(60): Show |
64 | HG00544.hp2 HG00673.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.5255-1617G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263358 | |||||||
chr6:159263452 | C | T | 2 | a0001c0006t0001g0053 a0001c0006t0001g0059 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.5255-1523C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263452 | |||||||
chr6:159263528 | C | T | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.5255-1447C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263528 | |||||||
chr6:159263552 | T | C | 263 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(260): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.5255-1423T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263552 | |||||||
chr6:159263553 | G | A | 1 | a0012c0037t0002g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5255-1422G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263553 | |||||||
chr6:159263564 | C | T | 1 | a0004c0003t0002g0097 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.5255-1411C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263564 | |||||||
chr6:159263620 | G | A | 2 | a0003c0001t0002g0277 a0004c0003t0002g0117 |
2 | NA18969.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.5255-1355G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263620 | |||||||
chr6:159263635 | G | C | 78 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(75): Show |
82 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.5255-1340G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263635 | |||||||
chr6:159263643 | T | A | 1 | a0023c0044t0001g0296 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5255-1332T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263643 | |||||||
chr6:159263686 | T | C | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5255-1289T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263686 | |||||||
chr6:159263694 | G | A | 2 | a0001c0005t0001g0087 a0002c0004t0007g0208 |
2 | HG01069.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.5255-1281G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263694 | |||||||
chr6:159263824 | G | A | 1 | a0011c0048t0002g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5255-1151G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263824 | |||||||
chr6:159263879 | T | C | 263 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(260): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.5255-1096T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263879 | |||||||
chr6:159263954 | T | TCAAA | 7 | a0005c0002t0001g0003 a0005c0002t0001g0027 a0005c0002t0001g0028 others(4): Show |
8 | HG02280.hp1 HG02572.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.5255-1004_5255-100 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 159263954 | ||||||
chr6:159263963 | C | A | 1 | a0002c0004t0001g0193 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5255-1012C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159263963 | |||||||
chr6:159264087 | G | A | 167 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(164): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.5255-888G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159264087 | |||||||
chr6:159264126 | A | G | 1 | a0004c0003t0002g0112 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.5255-849A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159264126 | |||||||
chr6:159264126 | A | T | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5255-849A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159264126 | |||||||
chr6:159264128 | G | A | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5255-847G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159264128 | |||||||
chr6:159264224 | T | C | 4 | a0003c0001t0002g0267 a0004c0003t0002g0041 a0004c0003t0002g0042 others(1): Show |
4 | HG00621.hp1 NA19011.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.5255-751T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159264224 | |||||||
chr6:159264266 | A | G | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5255-709A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159264266 | |||||||
chr6:159264269 | T | C | 1 | a0001c0005t0001g0048 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.5255-706T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159264269 | |||||||
chr6:159264465 | A | G | 4 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5255-510A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159264465 | |||||||
chr6:159264640 | C | T | 1 | a0005c0002t0001g0122 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.5255-335C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159264640 | |||||||
chr6:159264801 | T | C | 1 | a0001c0062t0001g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.5255-174T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 19/22 | chr6 | 159264801 | |||||||
chr6:159265145 | G | A | 78 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(75): Show |
82 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.5284+141G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265145 | |||||||
chr6:159265493 | C | T | 60 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0156 others(57): Show |
63 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.5284+489C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265493 | |||||||
chr6:159265550 | C | T | 1 | a0001c0010t0003g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5285-534C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265550 | |||||||
chr6:159265596 | C | G | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5285-488C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265596 | |||||||
chr6:159265618 | G | A | 7 | a0002c0018t0004g0175 a0003c0012t0004g0171 a0003c0012t0004g0185 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.5285-466G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265618 | |||||||
chr6:159265708 | T | C | 78 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(75): Show |
82 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.5285-376T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265708 | |||||||
chr6:159265756 | C | T | 3 | a0004c0020t0001g0099 a0004c0020t0001g0100 a0004c0020t0001g0107 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5285-328C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265756 | |||||||
chr6:159265796 | C | T | 78 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(75): Show |
82 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.5285-288C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265796 | |||||||
chr6:159265797 | G | A | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5285-287G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265797 | |||||||
chr6:159265830 | C | A | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5285-254C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265830 | |||||||
chr6:159265948 | A | G | 1 | a0028c0036t0003g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5285-136A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265948 | |||||||
chr6:159265949 | CACAA | C | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5285-117_5285-114d others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr6 | 159265949 | ||||||
chr6:159265982 | G | A | 1 | a0001c0006t0001g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5285-102G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265982 | |||||||
chr6:159265996 | A | G | 1 | a0008c0070t0005g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5285-88A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 20/22 | chr6 | 159265996 | |||||||
chr6:159266493 | G | A | 172 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(169): Show |
174 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.5446+248G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159266493 | |||||||
chr6:159266552 | T | C | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5446+307T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159266552 | |||||||
chr6:159266654 | T | C | 63 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(60): Show |
64 | HG00544.hp2 HG00673.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.5446+409T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159266654 | |||||||
chr6:159266680 | GT | G | 8 | a0003c0001t0002g0211 a0003c0001t0002g0213 a0003c0001t0002g0260 others(5): Show |
8 | HG00280.hp2 HG01934.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.5446+453delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 159266680 | ||||||
chr6:159266680 | GTT | G | 74 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(71): Show |
78 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.5446+452_5446+453d others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 159266680 | ||||||
chr6:159266680 | GTTT | G | 13 | a0001c0006t0001g0045 a0001c0063t0002g0285 a0003c0001t0002g0188 others(10): Show |
13 | HG00280.hp1 HG02109.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.5446+451_5446+453d others(5): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 159266680 | ||||||
chr6:159266680 | GTTTT | G | 101 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(98): Show |
102 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.5446+450_5446+453d others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 159266680 | ||||||
chr6:159266680 | GTTTTT | G | 60 | a0003c0045t0001g0192 a0005c0002t0001g0003 a0005c0002t0001g0014 others(57): Show |
61 | HG00544.hp2 HG00673.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.5446+449_5446+453d others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 159266680 | ||||||
chr6:159266684 | T | G | 1 | a0001c0006t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.5446+439T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159266684 | |||||||
chr6:159266685 | T | G | 98 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(95): Show |
99 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.5446+440T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159266685 | |||||||
chr6:159266686 | T | G | 1 | a0003c0045t0001g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5446+441T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159266686 | |||||||
chr6:159266909 | T | C | 1 | a0005c0002t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5446+664T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159266909 | |||||||
chr6:159266933 | G | A | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5446+688G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159266933 | |||||||
chr6:159267155 | T | C | 1 | a0005c0002t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5447-649T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159267155 | |||||||
chr6:159267156 | C | T | 1 | a0005c0002t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5447-648C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159267156 | |||||||
chr6:159267158 | T | C | 1 | a0005c0002t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5447-646T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159267158 | |||||||
chr6:159267214 | G | GTC | 3 | a0002c0004t0001g0164 a0002c0004t0001g0228 a0002c0004t0001g0275 |
3 | HG01256.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.5447-574_5447-573d others(4): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 159267214 | ||||||
chr6:159267442 | A | G | 2 | a0005c0002t0001g0133 a0006c0007t0001g0157 |
2 | NA18954.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.5447-362A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159267442 | |||||||
chr6:159267757 | G | T | 2 | a0005c0002t0001g0066 a0005c0002t0001g0119 |
2 | HG02155.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.5447-47G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 21/22 | chr6 | 159267757 | |||||||
chr6:159267972 | C | G | 132 | a0001c0010t0003g0013 a0001c0010t0003g0022 a0001c0010t0003g0043 others(129): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.5569+46C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159267972 | |||||||
chr6:159267999 | C | T | 7 | a0002c0018t0004g0175 a0003c0012t0004g0171 a0003c0012t0004g0185 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.5569+73C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159267999 | |||||||
chr6:159268017 | C | T | 78 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(75): Show |
82 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.5569+91C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268017 | |||||||
chr6:159268055 | C | A | 5 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5569+129C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268055 | |||||||
chr6:159268101 | C | T | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5569+175C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268101 | |||||||
chr6:159268146 | C | T | 2 | a0001c0005t0001g0087 a0002c0004t0007g0208 |
2 | HG01069.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.5569+220C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268146 | |||||||
chr6:159268271 | G | T | 1 | a0005c0002t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5569+345G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268271 | |||||||
chr6:159268273 | T | A | 1 | a0005c0002t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5569+347T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268273 | |||||||
chr6:159268402 | G | T | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5569+476G>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268402 | |||||||
chr6:159268423 | C | G | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5569+497C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268423 | |||||||
chr6:159268423 | C | T | 2 | a0015c0030t0003g0032 a0015c0030t0003g0033 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.5569+497C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268423 | |||||||
chr6:159268557 | C | A | 5 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5569+631C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268557 | |||||||
chr6:159268625 | A | T | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5569+699A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268625 | |||||||
chr6:159268634 | C | G | 3 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0049t0002g0159 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5569+708C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268634 | |||||||
chr6:159268655 | T | A | 1 | a0005c0002t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5569+729T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268655 | |||||||
chr6:159268666 | C | T | 1 | a0004c0067t0003g0131 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.5569+740C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268666 | |||||||
chr6:159268683 | T | TATCTA | 4 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+758_5569+762d others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268683 | ||||||
chr6:159268699 | CATCT | C | 3 | a0004c0053t0003g0034 a0006c0026t0001g0252 a0006c0026t0001g0253 |
3 | HG03491.hp2 HG03492.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5569+781_5569+784d others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268699 | ||||||
chr6:159268723 | C | CATCT | 65 | a0001c0005t0001g0082 a0002c0004t0001g0225 a0005c0002t0001g0003 others(62): Show |
66 | HG00544.hp2 HG00673.hp1 HG01109.hp2 others(63): Show |
intron_variant | MODIFIER | c.5569+813_5569+816d others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268723 | ||||||
chr6:159268723 | C | CATCTATC others(1): Show |
97 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(94): Show |
98 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.5569+809_5569+816d others(10): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268723 | ||||||
chr6:159268723 | C | CATCTATC others(5): Show |
3 | a0001c0005t0001g0090 a0005c0029t0001g0056 a0005c0029t0001g0061 |
3 | HG00733.hp1 HG00735.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.5569+805_5569+816d others(14): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268723 | ||||||
chr6:159268758 | T | G | 1 | a0005c0002t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5569+832T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268758 | |||||||
chr6:159268809 | CATCTATC others(29): Show |
C | 1 | a0033c0074t0001g0081 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.5569+894_5569+929d others(38): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268809 | ||||||
chr6:159268821 | C | CATCT | 6 | a0001c0010t0003g0284 a0003c0012t0004g0186 a0009c0013t0002g0031 others(3): Show |
6 | HG00741.hp2 HG01255.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.5569+935_5569+938d others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268821 | ||||||
chr6:159268821 | C | CATTT | 14 | a0002c0017t0002g0005 a0002c0017t0002g0182 a0003c0001t0002g0180 others(11): Show |
14 | HG00408.hp1 HG00673.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.5569+897_5569+898i others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268821 | ||||||
chr6:159268821 | CATCT | C | 45 | a0001c0010t0003g0286 a0001c0055t0003g0062 a0003c0001t0002g0006 others(42): Show |
46 | HG00140.hp2 HG00438.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.5569+935_5569+938d others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268821 | ||||||
chr6:159268821 | CATCTATC others(1): Show |
C | 15 | a0001c0010t0003g0013 a0001c0010t0003g0022 a0001c0010t0003g0043 others(12): Show |
15 | HG02055.hp1 HG02738.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.5569+931_5569+938d others(10): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268821 | ||||||
chr6:159268821 | CATCTATC others(5): Show |
C | 6 | a0001c0010t0003g0128 a0002c0018t0003g0219 a0002c0018t0003g0220 others(3): Show |
6 | HG00140.hp1 HG00639.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5569+927_5569+938d others(14): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268821 | ||||||
chr6:159268821 | CATCTATC others(17): Show |
C | 159 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(156): Show |
161 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.5569+915_5569+938d others(26): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268821 | ||||||
chr6:159268821 | CATCTATC others(21): Show |
C | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.5569+911_5569+938d others(30): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268821 | ||||||
chr6:159268824 | C | T | 22 | a0001c0057t0002g0024 a0003c0001t0002g0178 a0003c0001t0002g0211 others(19): Show |
23 | HG00280.hp2 HG00544.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.5569+898C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268824 | |||||||
chr6:159268828 | C | T | 33 | a0003c0001t0002g0006 a0003c0001t0002g0198 a0003c0001t0002g0203 others(30): Show |
34 | HG00140.hp2 HG00438.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.5569+902C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268828 | |||||||
chr6:159268832 | C | T | 8 | a0003c0001t0002g0188 a0003c0001t0002g0191 a0003c0001t0002g0215 others(5): Show |
8 | HG02055.hp1 HG02922.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.5569+906C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268832 | |||||||
chr6:159268836 | C | T | 1 | a0003c0001t0002g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5569+910C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268836 | |||||||
chr6:159268867 | T | C | 1 | a0001c0005t0001g0287 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5569+941T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268867 | |||||||
chr6:159268890 | ACTAT | A | 5 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5569+970_5569+973d others(6): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268890 | ||||||
chr6:159268990 | TTATC | T | 75 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(72): Show |
79 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.5569+1065_5569+106 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268990 | |||||||
chr6:159268991 | T | C | 2 | a0003c0001t0002g0260 a0003c0051t0002g0264 |
2 | HG00438.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.5569+1065T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159268991 | |||||||
chr6:159268991 | T | TATCC | 133 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0050 others(130): Show |
136 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.5569+1103_5569+110 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268991 | ||||||
chr6:159268991 | T | TATCCATC others(1): Show |
5 | a0001c0005t0001g0048 a0001c0006t0001g0084 a0001c0033t0001g0295 others(2): Show |
5 | HG02148.hp2 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.5569+1099_5569+110 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268991 | ||||||
chr6:159268991 | TATCC | T | 15 | a0001c0006t0001g0146 a0001c0010t0003g0013 a0001c0010t0003g0022 others(12): Show |
15 | HG01109.hp2 HG01243.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.5569+1103_5569+110 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159268991 | ||||||
chr6:159269029 | T | C | 1 | a0018c0047t0002g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5569+1103T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269029 | |||||||
chr6:159269034 | C | A | 1 | a0005c0002t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5569+1108C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269034 | |||||||
chr6:159269036 | A | C | 1 | a0005c0002t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5569+1110A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269036 | |||||||
chr6:159269044 | GTATCTAT others(21): Show |
G | 1 | a0005c0002t0001g0058 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5569+1132_5569+115 others(32): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269044 | ||||||
chr6:159269058 | G | GTCTA | 40 | a0001c0010t0003g0284 a0002c0017t0002g0005 a0002c0017t0002g0182 others(37): Show |
40 | HG00438.hp1 HG00544.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.5569+1171_5569+117 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269058 | ||||||
chr6:159269058 | GTCTA | G | 26 | a0001c0010t0003g0043 a0001c0055t0003g0062 a0001c0063t0002g0285 others(23): Show |
27 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.5569+1171_5569+117 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269058 | ||||||
chr6:159269058 | GTCTATCT others(1): Show |
G | 6 | a0001c0010t0003g0013 a0001c0010t0003g0022 a0001c0010t0003g0074 others(3): Show |
6 | HG00639.hp1 HG02698.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.5569+1167_5569+117 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269058 | ||||||
chr6:159269058 | GTCTATCT others(5): Show |
G | 1 | a0007c0009t0002g0274 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5569+1163_5569+117 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269058 | ||||||
chr6:159269058 | GTCTATCT others(13): Show |
G | 1 | a0006c0007t0001g0273 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5569+1155_5569+117 others(24): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269058 | ||||||
chr6:159269058 | GTCTATCT others(17): Show |
G | 163 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(160): Show |
165 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.5569+1151_5569+117 others(28): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269058 | ||||||
chr6:159269082 | A | G | 1 | a0005c0002t0001g0058 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5569+1156A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269082 | |||||||
chr6:159269156 | C | CTATG | 87 | a0001c0057t0002g0024 a0001c0063t0002g0285 a0002c0017t0002g0005 others(84): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.5569+1254_5569+125 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269156 | ||||||
chr6:159269156 | C | CTATGTAT others(1): Show |
30 | a0001c0010t0003g0074 a0001c0010t0003g0128 a0001c0010t0003g0284 others(27): Show |
31 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.5569+1250_5569+125 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269156 | ||||||
chr6:159269156 | C | CTATGTAT others(5): Show |
5 | a0001c0010t0003g0013 a0001c0010t0003g0022 a0001c0010t0003g0043 others(2): Show |
5 | HG02622.hp1 HG02738.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.5569+1246_5569+125 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269156 | ||||||
chr6:159269156 | CTATG | C | 7 | a0002c0018t0004g0175 a0003c0012t0004g0171 a0003c0012t0004g0185 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.5569+1254_5569+125 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269156 | ||||||
chr6:159269205 | A | ACATC | 22 | a0001c0005t0001g0073 a0001c0005t0001g0082 a0001c0005t0001g0094 others(19): Show |
23 | HG00280.hp1 HG00621.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.5569+1279_5569+128 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269205 | |||||||
chr6:159269205 | ATATC | A | 18 | a0001c0005t0001g0090 a0001c0005t0001g0139 a0001c0010t0003g0128 others(15): Show |
18 | HG01081.hp2 HG01256.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.5569+1320_5569+132 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269205 | ||||||
chr6:159269205 | ATATCTAT others(9): Show |
A | 1 | a0003c0001t0002g0218 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5569+1308_5569+132 others(20): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269205 | ||||||
chr6:159269205 | ATATCTAT others(13): Show |
A | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5569+1304_5569+132 others(24): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269205 | ||||||
chr6:159269206 | T | C | 126 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(123): Show |
127 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.5569+1280T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269206 | |||||||
chr6:159269210 | T | C | 15 | a0001c0005t0001g0090 a0001c0005t0001g0139 a0001c0061t0001g0092 others(12): Show |
15 | HG01081.hp2 HG01256.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.5569+1284T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269210 | |||||||
chr6:159269222 | T | C | 4 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+1296T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269222 | |||||||
chr6:159269229 | CT | C | 3 | a0011c0023t0002g0173 a0011c0023t0002g0177 a0011c0049t0002g0159 |
3 | HG02965.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5569+1304delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269229 | |||||||
chr6:159269230 | T | C | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5569+1304T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269230 | |||||||
chr6:159269234 | T | C | 77 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(74): Show |
81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.5569+1308T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269234 | |||||||
chr6:159269236 | TCTATCTA others(6): Show |
T | 1 | a0003c0046t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5569+1312_5569+132 others(17): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269236 | ||||||
chr6:159269238 | T | C | 11 | a0003c0001t0002g0232 a0003c0001t0002g0262 a0005c0002t0001g0044 others(8): Show |
11 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.5569+1312T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269238 | |||||||
chr6:159269238 | T | TATC | 7 | a0002c0017t0002g0182 a0003c0001t0002g0191 a0003c0001t0002g0226 others(4): Show |
7 | HG02523.hp1 HG02886.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.5569+1313_5569+131 others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269238 | ||||||
chr6:159269240 | TCTATCTA others(2): Show |
T | 3 | a0003c0001t0002g0006 a0003c0001t0002g0213 a0003c0001t0002g0214 |
4 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.5569+1316_5569+132 others(13): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269240 | ||||||
chr6:159269241 | C | CCATCTAT | 4 | a0004c0068t0004g0149 a0005c0002t0001g0060 a0005c0002t0001g0065 others(1): Show |
4 | HG02976.hp1 NA19064.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+1315_5569+131 others(11): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269241 | |||||||
chr6:159269241 | CT | C | 64 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0003c0001t0002g0156 others(61): Show |
67 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.5569+1316delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269241 | |||||||
chr6:159269241 | CTATCTAT others(13): Show |
C | 1 | a0018c0042t0002g0282 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5569+1316_5569+133 others(24): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269241 | |||||||
chr6:159269242 | T | C | 49 | a0002c0004t0001g0172 a0002c0004t0001g0176 a0002c0018t0004g0175 others(46): Show |
49 | HG00544.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.5569+1316T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269242 | |||||||
chr6:159269242 | T | TATC | 3 | a0003c0001t0002g0232 a0003c0001t0002g0262 a0005c0002t0001g0133 |
3 | HG04199.hp1 NA18954.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5569+1317_5569+131 others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269242 | ||||||
chr6:159269245 | CT | C | 4 | a0006c0007t0001g0157 a0009c0013t0002g0025 a0009c0013t0002g0026 others(1): Show |
4 | HG02615.hp1 NA18906.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.5569+1320delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269245 | |||||||
chr6:159269245 | CTATCCAT others(17): Show |
C | 1 | a0023c0044t0001g0296 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5569+1320_5569+134 others(28): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269245 | |||||||
chr6:159269246 | T | C | 16 | a0001c0055t0003g0062 a0005c0002t0001g0003 a0005c0002t0001g0027 others(13): Show |
17 | HG01255.hp1 HG01257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.5569+1320T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269246 | |||||||
chr6:159269246 | T | TATC | 9 | a0002c0018t0004g0175 a0003c0012t0004g0185 a0003c0012t0004g0186 others(6): Show |
9 | HG00544.hp2 HG01109.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.5569+1321_5569+132 others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269246 | ||||||
chr6:159269246 | TATCCATC others(4): Show |
T | 4 | a0008c0011t0002g0016 a0011c0023t0002g0173 a0011c0023t0002g0177 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+1324_5569+133 others(15): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269246 | ||||||
chr6:159269248 | TC | T | 36 | a0002c0004t0001g0172 a0002c0004t0001g0176 a0003c0012t0004g0171 others(33): Show |
36 | HG00673.hp1 HG01361.hp1 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.5569+1324delC | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269248 | ||||||
chr6:159269249 | C | CTAT | 11 | a0001c0055t0003g0062 a0005c0002t0001g0027 a0005c0002t0001g0028 others(8): Show |
11 | HG01255.hp1 HG01257.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.5569+1323_5569+132 others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269249 | |||||||
chr6:159269249 | CCATCTAT | C | 15 | a0003c0001t0002g0178 a0003c0001t0002g0215 a0003c0001t0002g0216 others(12): Show |
15 | HG00673.hp2 HG02055.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.5569+1332_5569+133 others(11): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269249 | ||||||
chr6:159269250 | C | T | 84 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(81): Show |
88 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.5569+1324C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269250 | |||||||
chr6:159269253 | CT | C | 5 | a0005c0002t0001g0003 a0005c0002t0001g0122 a0007c0052t0003g0222 others(2): Show |
6 | HG02258.hp2 HG02300.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.5569+1328delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269253 | |||||||
chr6:159269254 | TATC | T | 51 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0003c0001t0002g0006 others(48): Show |
55 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.5569+1332_5569+133 others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269254 | ||||||
chr6:159269257 | C | CATCT | 11 | a0001c0010t0003g0022 a0005c0002t0001g0038 a0005c0002t0001g0039 others(8): Show |
12 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.5569+1363_5569+136 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269257 | ||||||
chr6:159269257 | C | CATCTATC others(1): Show |
7 | a0001c0010t0003g0013 a0001c0010t0003g0286 a0004c0053t0003g0034 others(4): Show |
7 | HG02976.hp2 HG03041.hp2 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.5569+1359_5569+136 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269257 | ||||||
chr6:159269257 | C | CT | 82 | a0002c0004t0001g0172 a0002c0004t0001g0176 a0002c0017t0002g0182 others(79): Show |
83 | HG00544.hp2 HG01109.hp2 HG01243.hp2 others(80): Show |
intron_variant | MODIFIER | c.5569+1331_5569+133 others(5): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269257 | |||||||
chr6:159269257 | C | CTATCT | 4 | a0001c0055t0003g0062 a0005c0002t0001g0027 a0005c0002t0001g0067 others(1): Show |
4 | HG01255.hp1 HG02622.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.5569+1331_5569+133 others(9): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269257 | |||||||
chr6:159269257 | C | T | 15 | a0003c0001t0002g0178 a0003c0001t0002g0215 a0003c0001t0002g0216 others(12): Show |
15 | HG00673.hp2 HG02055.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.5569+1331C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269257 | |||||||
chr6:159269277 | T | C | 2 | a0002c0004t0001g0172 a0002c0004t0001g0176 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5569+1351T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269277 | |||||||
chr6:159269281 | T | C | 8 | a0001c0005t0001g0072 a0002c0004t0001g0172 a0002c0004t0001g0176 others(5): Show |
8 | HG01993.hp2 HG02145.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.5569+1355T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269281 | |||||||
chr6:159269281 | TATCTATC others(5): Show |
T | 3 | a0001c0005t0001g0287 a0003c0022t0001g0248 a0022c0056t0001g0124 |
3 | HG00741.hp1 HG02809.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.5569+1359_5569+137 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269281 | ||||||
chr6:159269285 | T | C | 95 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(92): Show |
96 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.5569+1359T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269285 | |||||||
chr6:159269289 | T | C | 92 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(89): Show |
93 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.5569+1363T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269289 | |||||||
chr6:159269293 | C | CTATCTAT others(2): Show |
5 | a0001c0005t0001g0072 a0002c0008t0001g0199 a0004c0020t0001g0099 others(2): Show |
5 | HG01993.hp2 HG02683.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.5569+1367_5569+136 others(13): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269293 | |||||||
chr6:159269293 | C | T | 154 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(151): Show |
156 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.5569+1367C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269293 | |||||||
chr6:159269296 | C | T | 2 | a0002c0004t0001g0172 a0002c0004t0001g0176 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5569+1370C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269296 | |||||||
chr6:159269297 | C | CT | 20 | a0001c0005t0001g0051 a0001c0005t0001g0073 a0001c0005t0001g0093 others(17): Show |
21 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.5569+1371_5569+137 others(5): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269297 | |||||||
chr6:159269297 | C | CTATCTAT others(2): Show |
59 | a0001c0005t0001g0015 a0001c0005t0001g0075 a0001c0005t0001g0082 others(56): Show |
59 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.5569+1371_5569+137 others(13): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269297 | |||||||
chr6:159269297 | C | CTATCTAT others(10): Show |
10 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(7): Show |
10 | HG00408.hp2 HG01069.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.5569+1371_5569+137 others(21): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269297 | |||||||
chr6:159269297 | C | T | 9 | a0001c0005t0001g0072 a0001c0005t0001g0079 a0002c0004t0001g0172 others(6): Show |
9 | HG01975.hp1 HG01993.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.5569+1371C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269297 | |||||||
chr6:159269299 | T | A | 5 | a0001c0005t0001g0072 a0002c0008t0001g0199 a0004c0020t0001g0099 others(2): Show |
5 | HG01993.hp2 HG02683.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.5569+1373T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269299 | |||||||
chr6:159269300 | C | T | 1 | a0003c0045t0001g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5569+1374C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269300 | |||||||
chr6:159269301 | C | T | 98 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(95): Show |
99 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.5569+1375C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269301 | |||||||
chr6:159269303 | T | A | 61 | a0001c0005t0001g0015 a0001c0005t0001g0075 a0001c0005t0001g0082 others(58): Show |
61 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.5569+1377T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269303 | |||||||
chr6:159269304 | C | T | 20 | a0001c0005t0001g0051 a0001c0005t0001g0073 a0001c0005t0001g0093 others(17): Show |
21 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.5569+1378C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269304 | |||||||
chr6:159269307 | T | A | 1 | a0003c0045t0001g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5569+1381T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269307 | |||||||
chr6:159269307 | T | TTTATCTA others(8): Show |
1 | a0001c0005t0001g0079 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5569+1381_5569+138 others(19): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269307 | |||||||
chr6:159269307 | TC | T | 17 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0050 others(14): Show |
18 | HG00408.hp2 HG01074.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.5569+1383delC | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269307 | ||||||
chr6:159269308 | C | CTAACTAT | 19 | a0001c0005t0001g0051 a0001c0005t0001g0073 a0001c0005t0001g0093 others(16): Show |
19 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.5569+1382_5569+138 others(11): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269308 | |||||||
chr6:159269308 | C | CTAT | 61 | a0001c0005t0001g0015 a0001c0005t0001g0075 a0001c0005t0001g0082 others(58): Show |
61 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.5569+1382_5569+138 others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269308 | |||||||
chr6:159269308 | C | T | 1 | a0001c0005t0001g0079 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5569+1382C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269308 | |||||||
chr6:159269312 | T | A | 1 | a0001c0006t0001g0004 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5569+1386T>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269312 | |||||||
chr6:159269317 | T | C | 99 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(96): Show |
100 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.5569+1391T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269317 | |||||||
chr6:159269324 | A | ACTATCTA others(13): Show |
4 | a0001c0005t0001g0287 a0003c0022t0001g0248 a0022c0056t0001g0124 others(1): Show |
4 | HG00741.hp1 HG01109.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.5569+1400_5569+141 others(24): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269324 | ||||||
chr6:159269324 | A | T | 99 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(96): Show |
100 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.5569+1398A>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269324 | |||||||
chr6:159269324 | ACTAT | A | 5 | a0002c0039t0002g0205 a0003c0001t0002g0178 a0012c0016t0002g0166 others(2): Show |
5 | HG02818.hp1 HG03195.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5569+1416_5569+141 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269324 | ||||||
chr6:159269329 | C | CTATCTAT others(9): Show |
62 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(59): Show |
63 | HG00544.hp2 HG00673.hp1 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.5569+1418_5569+141 others(20): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269329 | ||||||
chr6:159269329 | C | T | 1 | a0005c0002t0001g0150 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5569+1403C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269329 | |||||||
chr6:159269385 | A | C | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5569+1459A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269385 | |||||||
chr6:159269395 | ATCTG | A | 4 | a0005c0015t0001g0292 a0013c0024t0001g0190 a0013c0024t0001g0234 others(1): Show |
4 | HG00544.hp2 HG02071.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+1473_5569+147 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269395 | ||||||
chr6:159269397 | CTGTCTAT others(1): Show |
C | 59 | a0005c0002t0001g0003 a0005c0002t0001g0008 a0005c0002t0001g0014 others(56): Show |
60 | HG00673.hp1 HG01109.hp2 HG01361.hp1 others(57): Show |
intron_variant | MODIFIER | c.5569+1473_5569+148 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269397 | ||||||
chr6:159269401 | CTATG | C | 124 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(121): Show |
125 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.5569+1498_5569+150 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269401 | ||||||
chr6:159269424 | TGTAG | T | 78 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(75): Show |
82 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.5569+1502_5569+150 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269424 | ||||||
chr6:159269453 | C | T | 78 | a0001c0057t0002g0024 a0002c0017t0002g0005 a0002c0017t0002g0182 others(75): Show |
82 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.5569+1527C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269453 | |||||||
chr6:159269455 | C | CATCT | 13 | a0001c0006t0001g0148 a0002c0008t0001g0229 a0003c0001t0002g0198 others(10): Show |
13 | HG02055.hp1 HG03209.hp2 HG03239.hp1 others(10): Show |
intron_variant | MODIFIER | c.5569+1573_5569+157 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269455 | ||||||
chr6:159269455 | CATCT | C | 81 | a0001c0010t0003g0074 a0001c0010t0003g0128 a0001c0057t0002g0024 others(78): Show |
85 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.5569+1573_5569+157 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269455 | ||||||
chr6:159269455 | CATCTATC others(1): Show |
C | 11 | a0001c0010t0003g0286 a0003c0022t0001g0248 a0006c0007t0001g0161 others(8): Show |
11 | HG01255.hp1 HG02109.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.5569+1569_5569+157 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269455 | ||||||
chr6:159269455 | CATCTATC others(9): Show |
C | 1 | a0011c0023t0002g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5569+1561_5569+157 others(20): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269455 | ||||||
chr6:159269487 | T | C | 4 | a0008c0011t0002g0016 a0008c0070t0005g0036 a0011c0023t0002g0173 others(1): Show |
4 | HG02965.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+1561T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269487 | |||||||
chr6:159269487 | TATCTATC others(13): Show |
T | 1 | a0005c0002t0001g0003 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.5569+1565_5569+158 others(24): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269487 | ||||||
chr6:159269491 | T | C | 5 | a0002c0004t0001g0238 a0008c0011t0002g0016 a0008c0070t0005g0036 others(2): Show |
5 | HG02965.hp1 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.5569+1565T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269491 | |||||||
chr6:159269491 | T | TATCTATC others(17): Show |
1 | a0001c0006t0001g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5569+1572_5569+157 others(28): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269491 | ||||||
chr6:159269494 | CTATCTAT others(13): Show |
C | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5569+1569_5569+158 others(24): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269494 | |||||||
chr6:159269495 | T | C | 25 | a0001c0005t0001g0050 a0001c0006t0001g0004 a0001c0006t0001g0146 others(22): Show |
26 | HG00408.hp2 HG01256.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.5569+1569T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269495 | |||||||
chr6:159269495 | T | TATCCATC others(13): Show |
6 | a0001c0006t0001g0018 a0001c0033t0001g0295 a0002c0008t0001g0195 others(3): Show |
6 | HG03195.hp2 HG03453.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.5569+1572_5569+157 others(24): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269495 | ||||||
chr6:159269495 | TATCTATC others(13): Show |
T | 1 | a0004c0003t0002g0130 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5569+1573_5569+159 others(24): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269495 | ||||||
chr6:159269498 | C | CCATCCAT others(1): Show |
7 | a0001c0005t0001g0050 a0001c0006t0001g0004 a0002c0008t0001g0204 others(4): Show |
8 | HG00408.hp2 HG01516.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.5569+1572_5569+157 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269498 | |||||||
chr6:159269498 | C | G | 4 | a0008c0011t0002g0016 a0008c0070t0005g0036 a0011c0023t0002g0173 others(1): Show |
4 | HG02965.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+1572C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269498 | |||||||
chr6:159269498 | CTATCCAT others(9): Show |
C | 1 | a0003c0012t0004g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5569+1573_5569+158 others(20): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269498 | |||||||
chr6:159269499 | T | C | 103 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(100): Show |
104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.5569+1573T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269499 | |||||||
chr6:159269499 | T | TATCTATC others(21): Show |
1 | a0005c0002t0001g0030 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5569+1576_5569+157 others(32): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269499 | ||||||
chr6:159269502 | C | CCATCCAT others(1): Show |
25 | a0001c0005t0001g0048 a0001c0005t0001g0072 a0001c0005t0001g0073 others(22): Show |
25 | HG00438.hp2 HG00621.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.5569+1583_5569+158 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269502 | ||||||
chr6:159269502 | C | G | 1 | a0002c0004t0001g0238 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.5569+1576C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269502 | |||||||
chr6:159269502 | CCATCCAT others(5): Show |
C | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5569+1588_5569+159 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269502 | ||||||
chr6:159269503 | C | CATCCATG others(9): Show |
7 | a0001c0006t0001g0020 a0001c0006t0001g0059 a0001c0006t0001g0088 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.5569+1583_5569+158 others(20): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269503 | ||||||
chr6:159269503 | C | CATGCATC others(5): Show |
6 | a0001c0006t0001g0146 a0002c0008t0001g0231 a0005c0002t0001g0038 others(3): Show |
6 | HG01256.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.5569+1579_5569+158 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269503 | ||||||
chr6:159269503 | C | T | 1 | a0005c0002t0001g0030 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5569+1577C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269503 | |||||||
chr6:159269506 | C | CCATG | 17 | a0001c0005t0001g0047 a0001c0005t0001g0090 a0001c0005t0001g0094 others(14): Show |
17 | HG00544.hp2 HG00738.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.5569+1583_5569+158 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269506 | ||||||
chr6:159269506 | C | G | 5 | a0001c0010t0003g0286 a0002c0004t0001g0275 a0016c0031t0003g0289 others(2): Show |
5 | HG01361.hp2 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5569+1580C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269506 | |||||||
chr6:159269507 | C | CATGCATC others(5): Show |
21 | a0001c0005t0001g0015 a0001c0005t0001g0051 a0001c0005t0001g0082 others(18): Show |
21 | HG00280.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.5569+1583_5569+158 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269507 | ||||||
chr6:159269507 | C | T | 8 | a0001c0005t0001g0050 a0001c0006t0001g0004 a0002c0008t0001g0204 others(5): Show |
9 | HG00408.hp2 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.5569+1581C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269507 | |||||||
chr6:159269510 | C | G | 6 | a0002c0008t0001g0283 a0003c0001t0002g0250 a0004c0003t0002g0012 others(3): Show |
6 | HG02135.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.5569+1584C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269510 | |||||||
chr6:159269511 | C | T | 28 | a0001c0005t0001g0048 a0001c0005t0001g0072 a0001c0005t0001g0073 others(25): Show |
28 | HG00438.hp2 HG00621.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.5569+1585C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269511 | |||||||
chr6:159269514 | G | C | 110 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(107): Show |
112 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.5569+1588G>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269514 | |||||||
chr6:159269514 | G | GCATCCAT others(5): Show |
15 | a0001c0005t0001g0123 a0001c0005t0001g0142 a0001c0006t0001g0070 others(12): Show |
15 | HG00639.hp2 HG00738.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.5569+1596_5569+159 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269514 | ||||||
chr6:159269514 | G | GCATCCAT others(9): Show |
8 | a0001c0005t0001g0106 a0001c0005t0001g0139 a0001c0006t0001g0148 others(5): Show |
8 | HG01074.hp1 HG01169.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.5569+1596_5569+159 others(20): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269514 | ||||||
chr6:159269514 | G | GCATCCAT others(13): Show |
2 | a0005c0002t0001g0027 a0005c0015t0001g0291 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5569+1596_5569+159 others(24): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269514 | ||||||
chr6:159269514 | GCATC | G | 49 | a0001c0010t0003g0128 a0001c0010t0003g0284 a0001c0057t0002g0024 others(46): Show |
50 | HG00408.hp1 HG00438.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.5569+1641_5569+164 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269514 | ||||||
chr6:159269514 | GCATCCAT others(1): Show |
G | 12 | a0001c0010t0003g0022 a0002c0018t0004g0175 a0003c0001t0002g0233 others(9): Show |
14 | HG01257.hp1 HG02280.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.5569+1637_5569+164 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269514 | ||||||
chr6:159269515 | C | CATCCATC others(1): Show |
12 | a0001c0005t0001g0098 a0001c0005t0006g0137 a0003c0022t0001g0248 others(9): Show |
12 | HG00673.hp1 HG00733.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.5569+1596_5569+159 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269515 | ||||||
chr6:159269515 | C | T | 17 | a0001c0005t0001g0047 a0001c0005t0001g0090 a0001c0005t0001g0094 others(14): Show |
17 | HG00544.hp2 HG00738.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.5569+1589C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269515 | |||||||
chr6:159269519 | C | CATCT | 4 | a0005c0002t0001g0044 a0005c0002t0001g0151 a0006c0007t0001g0272 others(1): Show |
4 | HG01109.hp1 HG01109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+1596_5569+159 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269519 | ||||||
chr6:159269519 | C | T | 1 | a0002c0008t0001g0283 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5569+1593C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269519 | |||||||
chr6:159269522 | C | G | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5569+1596C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269522 | |||||||
chr6:159269523 | C | T | 24 | a0001c0005t0001g0287 a0005c0002t0001g0064 a0005c0002t0001g0066 others(21): Show |
24 | HG00741.hp1 HG02015.hp1 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.5569+1597C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269523 | |||||||
chr6:159269526 | C | G | 2 | a0002c0039t0002g0205 a0003c0012t0004g0186 |
2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5569+1600C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269526 | |||||||
chr6:159269527 | C | T | 2 | a0005c0002t0001g0054 a0006c0007t0001g0273 |
2 | HG01361.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.5569+1601C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269527 | |||||||
chr6:159269530 | C | G | 1 | a0004c0003t0002g0130 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5569+1604C>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269530 | |||||||
chr6:159269530 | C | T | 4 | a0001c0010t0003g0286 a0016c0031t0003g0289 a0016c0054t0003g0037 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.5569+1604C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269530 | |||||||
chr6:159269555 | C | A | 1 | a0005c0002t0001g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5569+1629C>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269555 | |||||||
chr6:159269555 | C | T | 1 | a0003c0001t0002g0211 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5569+1629C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269555 | |||||||
chr6:159269558 | CCATCCAT others(21): Show |
C | 1 | a0003c0001t0002g0211 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5569+1634_5569+166 others(32): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269558 | ||||||
chr6:159269567 | C | T | 1 | a0004c0067t0003g0131 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.5569+1641C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269567 | |||||||
chr6:159269571 | T | C | 30 | a0001c0005t0001g0287 a0002c0018t0003g0220 a0003c0001t0002g0260 others(27): Show |
30 | HG00140.hp1 HG00741.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.5569+1645T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269571 | |||||||
chr6:159269573 | TC | T | 3 | a0002c0018t0003g0220 a0004c0003t0002g0113 a0004c0067t0003g0131 |
3 | HG00140.hp1 NA18953.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.5569+1649delC | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269573 | ||||||
chr6:159269574 | C | CCAT | 23 | a0003c0001t0002g0260 a0005c0002t0001g0064 a0005c0002t0001g0066 others(20): Show |
23 | HG02015.hp1 HG02155.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.5569+1649_5569+165 others(7): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269574 | ||||||
chr6:159269575 | CT | C | 5 | a0001c0005t0001g0287 a0004c0053t0003g0034 a0008c0011t0003g0144 others(2): Show |
5 | HG00741.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5569+1650delT | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269575 | |||||||
chr6:159269576 | T | C | 1 | a0003c0001t0002g0260 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.5569+1650T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269576 | |||||||
chr6:159269577 | A | ATCTG | 6 | a0005c0002t0001g0058 a0006c0007t0001g0157 a0009c0013t0002g0025 others(3): Show |
6 | HG02109.hp2 HG02735.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.5569+1671_5569+167 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269577 | ||||||
chr6:159269577 | A | G | 1 | a0004c0067t0003g0131 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.5569+1651A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269577 | |||||||
chr6:159269577 | ATCTG | A | 7 | a0001c0062t0001g0083 a0003c0001t0002g0198 a0004c0003t0002g0097 others(4): Show |
7 | HG03486.hp1 NA18970.hp1 NA19011.hp1 others(4): Show |
intron_variant | MODIFIER | c.5569+1671_5569+167 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269577 | ||||||
chr6:159269578 | T | TC | 22 | a0005c0002t0001g0064 a0005c0002t0001g0066 a0005c0002t0001g0089 others(19): Show |
22 | HG02015.hp1 HG02155.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.5569+1653dupC | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269578 | ||||||
chr6:159269581 | G | A | 28 | a0001c0005t0001g0287 a0003c0001t0002g0260 a0004c0053t0003g0034 others(25): Show |
28 | HG00741.hp1 HG02015.hp1 HG02155.hp1 others(25): Show |
intron_variant | MODIFIER | c.5569+1655G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269581 | |||||||
chr6:159269582 | T | TC | 4 | a0001c0005t0001g0287 a0003c0001t0002g0260 a0009c0032t0003g0288 others(1): Show |
4 | HG00741.hp1 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+1657dupC | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269582 | ||||||
chr6:159269585 | G | A | 4 | a0001c0005t0001g0287 a0003c0001t0002g0260 a0009c0032t0003g0288 others(1): Show |
4 | HG00741.hp1 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+1659G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269585 | |||||||
chr6:159269589 | G | A | 3 | a0002c0018t0003g0220 a0004c0003t0002g0113 a0008c0011t0003g0144 |
3 | HG00140.hp1 HG02818.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.5569+1663G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269589 | |||||||
chr6:159269589 | GTCTGTCT others(5): Show |
G | 1 | a0004c0003t0002g0042 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.5569+1667_5569+167 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269589 | ||||||
chr6:159269589 | GTCTGTCT others(9): Show |
G | 4 | a0003c0046t0002g0243 a0004c0003t0002g0041 a0008c0028t0002g0118 others(1): Show |
4 | HG02258.hp2 NA18522.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.5569+1667_5569+168 others(20): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269589 | ||||||
chr6:159269589 | GTCTGTCT others(21): Show |
G | 1 | a0001c0063t0002g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5569+1667_5569+169 others(32): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269589 | ||||||
chr6:159269593 | G | A | 1 | a0004c0053t0003g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5569+1667G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269593 | |||||||
chr6:159269593 | GTCTGTCT others(1): Show |
G | 10 | a0001c0057t0002g0024 a0003c0001t0002g0006 a0003c0001t0002g0218 others(7): Show |
10 | HG00621.hp1 HG00735.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.5569+1671_5569+167 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269593 | ||||||
chr6:159269593 | GTCTGTCT others(5): Show |
G | 58 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0010t0003g0013 others(55): Show |
61 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.5569+1671_5569+168 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269593 | ||||||
chr6:159269593 | GTCTGTCT others(9): Show |
G | 4 | a0003c0001t0002g0180 a0003c0001t0002g0250 a0004c0003t0002g0017 others(1): Show |
4 | HG01978.hp2 HG02723.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.5569+1671_5569+168 others(20): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269593 | ||||||
chr6:159269593 | GTCTGTCT others(13): Show |
G | 1 | a0003c0001t0002g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5569+1671_5569+169 others(24): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269593 | ||||||
chr6:159269597 | G | A | 4 | a0003c0001t0002g0227 a0004c0019t0001g0063 a0004c0067t0003g0131 others(1): Show |
4 | HG02015.hp2 HG03209.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.5569+1671G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269597 | |||||||
chr6:159269597 | GTCTA | G | 63 | a0001c0005t0001g0073 a0001c0005t0001g0075 a0001c0005t0001g0090 others(60): Show |
65 | HG00544.hp2 HG00738.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.5570-1678_5570-167 others(8): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269597 | ||||||
chr6:159269597 | GTCTATCT others(1): Show |
G | 76 | a0001c0005t0001g0048 a0001c0005t0001g0050 a0001c0005t0001g0051 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.5570-1682_5570-167 others(12): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269597 | ||||||
chr6:159269597 | GTCTATCT others(5): Show |
G | 9 | a0002c0004t0001g0210 a0002c0004t0001g0221 a0002c0018t0004g0175 others(6): Show |
9 | HG01081.hp2 HG01891.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.5570-1686_5570-167 others(16): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269597 | ||||||
chr6:159269597 | GTCTATCT others(17): Show |
G | 1 | a0002c0039t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5570-1698_5570-167 others(28): Show |
FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 159269597 | ||||||
chr6:159269601 | A | G | 45 | a0001c0005t0001g0287 a0002c0018t0003g0220 a0003c0001t0002g0211 others(42): Show |
45 | HG00140.hp1 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.5569+1675A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269601 | |||||||
chr6:159269605 | A | G | 72 | a0001c0005t0001g0090 a0001c0005t0001g0287 a0001c0005t0006g0137 others(69): Show |
72 | HG00140.hp1 HG00544.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.5569+1679A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269605 | |||||||
chr6:159269609 | A | G | 4 | a0004c0053t0003g0034 a0005c0002t0001g0014 a0005c0002t0001g0151 others(1): Show |
4 | HG02523.hp2 HG02970.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.5569+1683A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269609 | |||||||
chr6:159269670 | G | A | 2 | a0001c0063t0002g0285 a0003c0046t0002g0243 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5570-1657G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269670 | |||||||
chr6:159269912 | A | C | 1 | a0004c0003t0002g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.5570-1415A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159269912 | |||||||
chr6:159270240 | G | A | 1 | a0001c0005t0001g0047 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.5570-1087G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159270240 | |||||||
chr6:159270563 | G | A | 1 | a0008c0011t0003g0057 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5570-764G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159270563 | |||||||
chr6:159270573 | G | A | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5570-754G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159270573 | |||||||
chr6:159270590 | A | G | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5570-737A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159270590 | |||||||
chr6:159270625 | T | C | 270 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(267): Show |
276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.5570-702T>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159270625 | |||||||
chr6:159270667 | C | T | 5 | a0003c0045t0001g0192 a0004c0020t0001g0099 a0004c0020t0001g0100 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.5570-660C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159270667 | |||||||
chr6:159270706 | T | G | 1 | a0001c0005t0001g0287 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5570-621T>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159270706 | |||||||
chr6:159270867 | G | A | 5 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5570-460G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159270867 | |||||||
chr6:159270878 | A | C | 5 | a0002c0039t0002g0205 a0009c0013t0002g0025 a0009c0013t0002g0026 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5570-449A>C | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159270878 | |||||||
chr6:159271016 | A | G | 3 | a0004c0020t0001g0099 a0004c0020t0001g0100 a0004c0020t0001g0107 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5570-311A>G | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159271016 | |||||||
chr6:159271289 | G | A | 165 | a0001c0005t0001g0015 a0001c0005t0001g0047 a0001c0005t0001g0048 others(162): Show |
167 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.5570-38G>A | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159271289 | |||||||
chr6:159271297 | C | T | 2 | a0006c0007t0001g0158 a0036c0071t0001g0035 |
2 | NA18948.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.5570-30C>T | FNDC1 | ENSG00000164694.17 | transcript | ENST00000297267.14 | protein_coding | 22/22 | chr6 | 159271297 |