Item | Value |
---|---|
geneid | 63923 |
ensemblid | ENSG00000120332.17 |
hgncid | 22942 |
symbol | TNN |
name | tenascin N |
refseq_nuc | NM_022093.2 |
refseq_prot | NP_071376.1 |
ensembl_nuc | ENST00000239462.9 |
ensembl_prot | ENSP00000239462.4 |
mane_status | MANE Select |
chr | chr1 |
start | 175067833 |
end | 175148075 |
strand | + |
ver | v1.2 |
region | chr1:175067833-175148075 |
region5000 | chr1:175062833-175153075 |
regionname0 | TNN_chr1_175067833_175148075 |
regionname5000 | TNN_chr1_175062833_175153075 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1299 | 52 | 25 | 11 | 5 | 4 | 7 | 3 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0002 | 0/0 | 1299 | 41 | 24 | 6 | 4 | 4 | 3 | 2 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0003 | 0/0 | 1299 | 34 | 1 | 0 | 26 | 2 | 5 | 24 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0004 | 1/1 | 1299 | 24 | 1 | 4 | 15 | 0 | 2 | 11 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0005 | 0/0 | 1299 | 24 | 0 | 7 | 17 | 0 | 0 | 14 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0006 | 0/0 | 1299 | 21 | 0 | 8 | 10 | 0 | 3 | 7 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0007 | 0/0 | 1299 | 20 | 10 | 1 | 3 | 1 | 5 | 3 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0008 | 0/0 | 1299 | 18 | 0 | 0 | 16 | 1 | 1 | 13 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0009 | 0/0 | 1299 | 14 | 0 | 3 | 5 | 2 | 4 | 5 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0010 | 0/0 | 1299 | 13 | 1 | 4 | 8 | 0 | 0 | 6 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0011 | 0/0 | 1299 | 11 | 0 | 5 | 5 | 1 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0012 | 0/0 | 1299 | 9 | 0 | 1 | 8 | 0 | 0 | 6 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0013 | 0/0 | 1299 | 8 | 6 | 1 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0014 | 0/0 | 1299 | 7 | 1 | 2 | 1 | 0 | 3 | 1 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0015 | 0/0 | 1299 | 7 | 3 | 0 | 3 | 0 | 1 | 3 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0016 | 0/0 | 1299 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0017 | 0/0 | 1299 | 5 | 0 | 2 | 3 | 0 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0018 | 0/0 | 1299 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0019 | 0/0 | 1299 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0020 | 0/0 | 1299 | 4 | 0 | 0 | 3 | 0 | 1 | 2 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0021 | 0/0 | 1299 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0022 | 0/0 | 1299 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0023 | 0/0 | 1299 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0024 | 0/0 | 1299 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0025 | 0/0 | 1299 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0026 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0027 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0028 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0029 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0030 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0031 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0032 | 0/0 | 1211 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1206): Show |
chr1 | 175062833 | 175153075 |
a0033 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0034 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0035 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0036 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0037 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0038 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0039 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0040 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0041 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MFRFP others(1289): Show |
chr1 | 175062833 | 175153075 |
a0042 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0043 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MFRFP others(1289): Show |
chr1 | 175062833 | 175153075 |
a0044 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0045 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0046 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0047 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0048 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0049 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0050 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0051 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0052 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0053 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0054 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0055 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0056 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0057 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
a0058 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | MSLQE others(1294): Show |
chr1 | 175062833 | 175153075 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3897 | 32 | 12 | 8 | 4 | 3 | 5 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0001c0016 | 0/0 | 3897 | 6 | 4 | 1 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0001c0028 | 0/0 | 3897 | 3 | 3 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0001c0031 | 0/0 | 3897 | 3 | 2 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0001c0036 | 0/0 | 3897 | 2 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0001c0042 | 0/0 | 3897 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0001c0073 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0001c0080 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0001c0081 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0001c0087 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0002c0005 | 0/0 | 3897 | 16 | 4 | 3 | 4 | 3 | 2 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0002c0009 | 0/0 | 3897 | 15 | 12 | 1 | 0 | 1 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0002c0026 | 0/0 | 3897 | 4 | 2 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0002c0029 | 0/0 | 3897 | 3 | 3 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0002c0037 | 0/0 | 3897 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0002c0077 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0003c0002 | 0/0 | 3897 | 26 | 1 | 0 | 19 | 1 | 5 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0003c0015 | 0/0 | 3897 | 7 | 0 | 0 | 7 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0003c0047 | 0/0 | 3897 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0004c0008 | 0/0 | 3897 | 15 | 0 | 2 | 12 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0004c0019 | 0/0 | 3897 | 5 | 1 | 1 | 2 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0004c0032 | 1/0 | 3897 | 2 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0004c0053 | 0/1 | 3897 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0004c0054 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0005c0003 | 0/0 | 3897 | 22 | 0 | 7 | 15 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0005c0055 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0005c0059 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0006c0004 | 0/0 | 3897 | 18 | 0 | 7 | 8 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0006c0044 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0006c0060 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0006c0061 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0007c0006 | 0/0 | 3897 | 16 | 8 | 1 | 3 | 1 | 3 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0007c0038 | 0/0 | 3897 | 2 | 1 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0007c0072 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0007c0079 | 0/0 | 3897 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0008c0007 | 0/0 | 3897 | 16 | 0 | 0 | 14 | 1 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0008c0040 | 0/0 | 3897 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0009c0012 | 0/0 | 3897 | 9 | 0 | 1 | 4 | 0 | 4 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0009c0021 | 0/0 | 3897 | 4 | 0 | 2 | 0 | 2 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0009c0049 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0010c0010 | 0/0 | 3897 | 13 | 1 | 4 | 8 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0011c0011 | 0/0 | 3897 | 11 | 0 | 5 | 5 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0012c0013 | 0/0 | 3897 | 9 | 0 | 1 | 8 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0013c0014 | 0/0 | 3897 | 8 | 6 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0014c0017 | 0/0 | 3897 | 6 | 0 | 2 | 1 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0014c0090 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0015c0024 | 0/0 | 3897 | 4 | 3 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0015c0030 | 0/0 | 3897 | 3 | 0 | 0 | 2 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0016c0018 | 0/0 | 3897 | 5 | 0 | 0 | 4 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0017c0025 | 0/0 | 3897 | 4 | 0 | 1 | 3 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0017c0074 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0018c0020 | 0/0 | 3897 | 5 | 0 | 0 | 5 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0019c0023 | 0/0 | 3897 | 4 | 4 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0020c0022 | 0/0 | 3897 | 4 | 0 | 0 | 3 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0021c0056 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0021c0057 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0021c0058 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0022c0027 | 0/0 | 3897 | 3 | 0 | 0 | 0 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0023c0041 | 0/0 | 3897 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0024c0035 | 0/0 | 3897 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0025c0033 | 0/0 | 3897 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0026c0034 | 0/0 | 3897 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0027c0039 | 0/0 | 3897 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0028c0043 | 0/0 | 3897 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0029c0082 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0030c0045 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0031c0068 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0032c0066 | 0/0 | 3633 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3628): Show |
chr1 | 175062833 | 175153075 | ||
a0033c0067 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0034c0089 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0035c0063 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0036c0076 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0037c0051 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0038c0085 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0039c0070 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0040c0065 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0041c0094 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATTAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0042c0071 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0043c0093 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATTAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0044c0069 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0045c0088 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0046c0091 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0047c0050 | 0/0 | 3897 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0048c0075 | 0/0 | 3897 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0049c0084 | 0/0 | 3897 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0050c0064 | 0/0 | 3897 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0051c0046 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0052c0086 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0053c0092 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0054c0083 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0055c0048 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0056c0052 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0057c0078 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 | ||
a0058c0062 | 0/0 | 3897 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | ATGAG others(3892): Show |
chr1 | 175062833 | 175153075 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5042 | 30 | 12 | 8 | 4 | 1 | 5 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0001t0002 | 0/0 | 5042 | 2 | 0 | 0 | 0 | 2 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0016t0001 | 0/0 | 5042 | 5 | 3 | 1 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0016t0008 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0028t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0028t0007 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0031t0005 | 0/0 | 5042 | 3 | 2 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0036t0001 | 0/0 | 5042 | 2 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0042t0001 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0073t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0080t0008 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0081t0001 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0001c0087t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0005t0001 | 0/0 | 5042 | 3 | 1 | 0 | 0 | 2 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0005t0002 | 0/0 | 5042 | 5 | 0 | 0 | 3 | 1 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0005t0003 | 0/0 | 5042 | 5 | 1 | 3 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0005t0004 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0005t0007 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0005t0016 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0009t0001 | 0/0 | 5042 | 9 | 9 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0009t0002 | 0/0 | 5042 | 2 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0009t0003 | 0/0 | 5042 | 3 | 2 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0009t0013 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0026t0001 | 0/0 | 5042 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0026t0003 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0029t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0029t0003 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0037t0003 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0002c0077t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0003c0002t0001 | 0/0 | 5042 | 25 | 1 | 0 | 19 | 1 | 4 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0003c0002t0012 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0003c0015t0001 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0003c0015t0003 | 0/0 | 5042 | 5 | 0 | 0 | 5 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0003c0047t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0004c0008t0001 | 0/0 | 5042 | 3 | 0 | 0 | 3 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0004c0008t0002 | 0/0 | 5042 | 10 | 0 | 0 | 9 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0004c0008t0003 | 0/0 | 5042 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0004c0019t0001 | 0/0 | 5042 | 4 | 1 | 1 | 1 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0004c0019t0002 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0004c0032t0002 | 1/0 | 5042 | 2 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0004c0053t0001 | 0/1 | 5042 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0004c0054t0002 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0005c0003t0001 | 0/0 | 5042 | 19 | 0 | 6 | 13 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0005c0003t0002 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0005c0003t0003 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0005c0055t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0005c0059t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0006c0004t0001 | 0/0 | 5042 | 17 | 0 | 7 | 7 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0006c0004t0002 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0006c0044t0014 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0006c0060t0003 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0006c0061t0002 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0007c0006t0001 | 0/0 | 5042 | 14 | 6 | 1 | 3 | 1 | 3 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0007c0006t0004 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0007c0006t0015 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0007c0038t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0007c0038t0011 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0007c0072t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0007c0079t0003 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0008c0007t0001 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0008c0007t0002 | 0/0 | 5042 | 14 | 0 | 0 | 12 | 1 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0008c0040t0003 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0009c0012t0002 | 0/0 | 5042 | 8 | 0 | 0 | 4 | 0 | 4 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0009c0012t0003 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0009c0021t0001 | 0/0 | 5042 | 4 | 0 | 2 | 0 | 2 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0009c0049t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0010c0010t0001 | 0/0 | 5042 | 13 | 1 | 4 | 8 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0011c0011t0001 | 0/0 | 5042 | 10 | 0 | 5 | 4 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0011c0011t0003 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0012c0013t0001 | 0/0 | 5042 | 9 | 0 | 1 | 8 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0013c0014t0001 | 0/0 | 5042 | 8 | 6 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0014c0017t0001 | 0/0 | 5042 | 6 | 0 | 2 | 1 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0014c0090t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0015c0024t0001 | 0/0 | 5042 | 3 | 3 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0015c0024t0002 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0015c0030t0001 | 0/0 | 5042 | 3 | 0 | 0 | 2 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0016c0018t0001 | 0/0 | 5042 | 5 | 0 | 0 | 4 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0017c0025t0001 | 0/0 | 5042 | 4 | 0 | 1 | 3 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0017c0074t0001 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0018c0020t0001 | 0/0 | 5042 | 5 | 0 | 0 | 5 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0019c0023t0001 | 0/0 | 5042 | 4 | 4 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0020c0022t0001 | 0/0 | 5042 | 4 | 0 | 0 | 3 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0021c0056t0006 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0021c0057t0001 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0021c0058t0006 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0022c0027t0001 | 0/0 | 5042 | 3 | 0 | 0 | 0 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0023c0041t0002 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0024c0035t0001 | 0/0 | 5042 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0025c0033t0001 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0026c0034t0003 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0027c0039t0009 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0028c0043t0001 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0029c0082t0001 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0030c0045t0001 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0031c0068t0002 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0032c0066t0001 | 0/0 | 4778 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(4773): Show |
chr1 | 175062833 | 175153075 |
a0033c0067t0006 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0034c0089t0003 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0035c0063t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0036c0076t0003 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0037c0051t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0038c0085t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0039c0070t0004 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0040c0065t0010 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0041c0094t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0042c0071t0004 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0043c0093t0003 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0044c0069t0004 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0045c0088t0005 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0046c0091t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0047c0050t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0048c0075t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0049c0084t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0050c0064t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0051c0046t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0052c0086t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0053c0092t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0054c0083t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0055c0048t0002 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0056c0052t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0057c0078t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
a0058c0062t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | GAGAC others(5037): Show |
chr1 | 175062833 | 175153075 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0016t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0016t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0016t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0016t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0016t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0016t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0028t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0028t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0028t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0031t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0031t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0031t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0036t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0036t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0042t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0042t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0073t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0080t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0081t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0001c0087t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0005t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0002g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0003g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0009t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0026t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0026t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0026t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0029t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0029t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0029t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0037t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0037t0003g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0002c0077t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0002t0012g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0015t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0015t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0015t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0015t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0015t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0015t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0015t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0003c0047t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0008t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0019t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0019t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0019t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0019t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0019t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0032t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0032t0002g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0053t0001g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0004c0054t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0003t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0055t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0005c0059t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0004t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0044t0014g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0060t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0006c0061t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0006t0015g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0038t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0038t0011g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0072t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0007c0079t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0007t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0040t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0008c0040t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0012t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0012t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0012t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0012t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0012t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0012t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0012t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0012t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0021t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0021t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0021t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0021t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0009c0049t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0010c0010t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0011c0011t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0012c0013t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0012c0013t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0012c0013t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0012c0013t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0012c0013t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0012c0013t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0012c0013t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0012c0013t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0012c0013t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0013c0014t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0013c0014t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0013c0014t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0013c0014t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0013c0014t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0013c0014t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0013c0014t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0013c0014t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0014c0017t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0014c0017t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0014c0017t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0014c0017t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0014c0017t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0014c0090t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0015c0024t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0015c0024t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0015c0024t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0015c0024t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0015c0030t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0015c0030t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0015c0030t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0016c0018t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0016c0018t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0016c0018t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0016c0018t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0016c0018t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0017c0025t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0017c0025t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0017c0025t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0017c0025t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0017c0074t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0018c0020t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0018c0020t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0018c0020t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0018c0020t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0018c0020t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0019c0023t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0019c0023t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0019c0023t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0019c0023t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0020c0022t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0020c0022t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0020c0022t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0020c0022t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0021c0056t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0021c0057t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0021c0058t0006g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0022c0027t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0022c0027t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0022c0027t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0023c0041t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0023c0041t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0024c0035t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0024c0035t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0025c0033t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0025c0033t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0026c0034t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0026c0034t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0027c0039t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0027c0039t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0028c0043t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0028c0043t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0029c0082t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0030c0045t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0031c0068t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0032c0066t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0033c0067t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0034c0089t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0035c0063t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0036c0076t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0037c0051t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0038c0085t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0039c0070t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0040c0065t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0041c0094t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0042c0071t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0043c0093t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0044c0069t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0045c0088t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0046c0091t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0047c0050t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0048c0075t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0049c0084t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0050c0064t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0051c0046t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0052c0086t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0053c0092t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0054c0083t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0055c0048t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0056c0052t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0057c0078t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
a0058c0062t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0122 | EUR | GBR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00099 | hp2 | a0007 | c0006 | t0001 | g0340 | EUR | GBR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00140 | hp1 | a0002 | c0005 | t0001 | g0114 | EUR | GBR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00140 | hp2 | a0008 | c0007 | t0002 | g0099 | EUR | GBR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00280 | hp1 | a0003 | c0002 | t0001 | g0278 | EUR | FIN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00280 | hp2 | a0011 | c0011 | t0001 | g0215 | EUR | FIN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00323 | hp1 | a0003 | c0047 | t0001 | g0293 | EUR | FIN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00323 | hp2 | a0002 | c0005 | t0001 | g0121 | EUR | FIN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00408 | hp1 | a0011 | c0011 | t0001 | g0238 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00408 | hp2 | a0010 | c0010 | t0001 | g0078 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00438 | hp1 | a0002 | c0005 | t0016 | g0030 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00438 | hp2 | a0006 | c0004 | t0001 | g0253 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00544 | hp1 | a0016 | c0018 | t0001 | g0290 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00544 | hp2 | a0008 | c0007 | t0002 | g0143 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00609 | hp1 | a0003 | c0002 | t0001 | g0303 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00609 | hp2 | a0023 | c0041 | t0002 | g0080 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00639 | hp1 | a0009 | c0021 | t0001 | g0004 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00639 | hp2 | a0011 | c0011 | t0001 | g0220 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00642 | hp1 | a0004 | c0032 | t0002 | g0192 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00642 | hp2 | a0029 | c0082 | t0001 | g0067 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00738 | hp1 | a0024 | c0035 | t0001 | g0216 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG00738 | hp2 | a0006 | c0004 | t0001 | g0191 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01069 | hp1 | a0021 | c0057 | t0001 | g0175 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01069 | hp2 | a0006 | c0004 | t0001 | g0243 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01070 | hp1 | a0030 | c0045 | t0001 | g0207 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01070 | hp2 | a0002 | c0026 | t0001 | g0002 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01071 | hp1 | a0002 | c0026 | t0001 | g0002 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01071 | hp2 | a0006 | c0004 | t0001 | g0245 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01074 | hp1 | a0006 | c0061 | t0002 | g0217 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01081 | hp1 | a0031 | c0068 | t0002 | g0034 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01106 | hp2 | a0001 | c0036 | t0001 | g0342 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01109 | hp1 | a0014 | c0017 | t0001 | g0127 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01109 | hp2 | a0009 | c0012 | t0003 | g0273 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01167 | hp1 | a0007 | c0006 | t0001 | g0349 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01167 | hp2 | a0011 | c0011 | t0001 | g0219 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01168 | hp1 | a0011 | c0011 | t0001 | g0190 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01168 | hp2 | a0002 | c0009 | t0002 | g0363 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01192 | hp1 | a0002 | c0005 | t0003 | g0105 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01192 | hp2 | a0001 | c0081 | t0001 | g0159 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01243 | hp1 | a0017 | c0025 | t0001 | g0109 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01243 | hp2 | a0017 | c0074 | t0001 | g0035 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01255 | hp2 | a0005 | c0003 | t0001 | g0212 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01256 | hp1 | a0006 | c0004 | t0001 | g0182 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01256 | hp2 | a0005 | c0003 | t0001 | g0169 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01257 | hp1 | a0010 | c0010 | t0001 | g0110 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01257 | hp2 | a0012 | c0013 | t0001 | g0101 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01258 | hp1 | a0010 | c0010 | t0001 | g0112 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01258 | hp2 | a0005 | c0003 | t0001 | g0181 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01261 | hp1 | a0032 | c0066 | t0001 | g0250 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01261 | hp2 | a0001 | c0016 | t0001 | g0362 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01346 | hp1 | a0006 | c0004 | t0001 | g0244 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01358 | hp1 | a0013 | c0014 | t0001 | g0056 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01358 | hp2 | a0009 | c0021 | t0001 | g0276 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0352 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01361 | hp2 | a0005 | c0003 | t0001 | g0257 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01433 | hp1 | a0011 | c0011 | t0001 | g0260 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01433 | hp2 | a0004 | c0008 | t0003 | g0247 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01496 | hp1 | a0006 | c0004 | t0001 | g0251 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01496 | hp2 | a0014 | c0017 | t0001 | g0001 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01515 | hp1 | a0009 | c0021 | t0001 | g0271 | EUR | IBS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01515 | hp2 | a0002 | c0005 | t0002 | g0117 | EUR | IBS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01517 | hp1 | a0009 | c0021 | t0001 | g0272 | EUR | IBS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01517 | hp2 | a0001 | c0016 | t0001 | g0360 | EUR | IBS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01884 | hp1 | a0001 | c0031 | t0005 | g0156 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01891 | hp1 | a0002 | c0005 | t0004 | g0009 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01891 | hp2 | a0013 | c0014 | t0001 | g0083 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01928 | hp1 | a0010 | c0010 | t0001 | g0113 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01928 | hp2 | a0005 | c0003 | t0001 | g0176 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01934 | hp1 | a0005 | c0003 | t0003 | g0256 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01934 | hp2 | a0010 | c0010 | t0001 | g0111 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01943 | hp1 | a0033 | c0067 | t0006 | g0100 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01943 | hp2 | a0002 | c0005 | t0003 | g0106 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01975 | hp1 | a0034 | c0089 | t0003 | g0103 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01975 | hp2 | a0004 | c0019 | t0001 | g0353 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01978 | hp1 | a0005 | c0003 | t0001 | g0188 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01978 | hp2 | a0004 | c0008 | t0003 | g0246 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01993 | hp1 | a0024 | c0035 | t0001 | g0214 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01993 | hp2 | a0002 | c0005 | t0003 | g0104 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02015 | hp1 | a0012 | c0013 | t0001 | g0070 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02015 | hp2 | a0004 | c0008 | t0001 | g0228 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02040 | hp1 | a0025 | c0033 | t0001 | g0236 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02040 | hp2 | a0010 | c0010 | t0001 | g0065 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02055 | hp1 | a0035 | c0063 | t0001 | g0268 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02055 | hp2 | a0002 | c0009 | t0001 | g0047 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02071 | hp1 | a0008 | c0007 | t0002 | g0058 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02083 | hp1 | a0011 | c0011 | t0003 | g0189 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02083 | hp2 | a0006 | c0004 | t0001 | g0249 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02129 | hp1 | a0037 | c0051 | t0001 | g0282 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02129 | hp2 | a0004 | c0054 | t0002 | g0193 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02132 | hp1 | a0005 | c0003 | t0001 | g0232 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02132 | hp2 | a0008 | c0007 | t0002 | g0130 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02135 | hp1 | a0004 | c0019 | t0002 | g0237 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02135 | hp2 | a0002 | c0005 | t0002 | g0347 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02145 | hp1 | a0021 | c0058 | t0006 | g0316 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02145 | hp2 | a0038 | c0085 | t0001 | g0335 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02155 | hp1 | a0005 | c0003 | t0001 | g0187 | EAS | CDX | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02155 | hp2 | a0012 | c0013 | t0001 | g0061 | EAS | CDX | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02165 | hp1 | a0006 | c0004 | t0001 | g0195 | EAS | CDX | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02257 | hp1 | a0002 | c0005 | t0003 | g0150 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02257 | hp2 | a0002 | c0009 | t0001 | g0042 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02280 | hp1 | a0007 | c0006 | t0001 | g0337 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02280 | hp2 | a0021 | c0056 | t0006 | g0274 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02300 | hp1 | a0011 | c0011 | t0001 | g0240 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02451 | hp1 | a0027 | c0039 | t0009 | g0012 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02451 | hp2 | a0007 | c0006 | t0001 | g0084 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02523 | hp1 | a0003 | c0002 | t0001 | g0297 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02523 | hp2 | a0004 | c0008 | t0002 | g0206 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02572 | hp1 | a0002 | c0009 | t0003 | g0361 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02572 | hp2 | a0001 | c0073 | t0001 | g0052 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02602 | hp1 | a0003 | c0002 | t0001 | g0279 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02602 | hp2 | a0014 | c0017 | t0001 | g0001 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02615 | hp1 | a0019 | c0023 | t0001 | g0174 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02615 | hp2 | a0001 | c0016 | t0001 | g0355 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02622 | hp1 | a0039 | c0070 | t0004 | g0015 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02622 | hp2 | a0040 | c0065 | t0010 | g0166 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02630 | hp1 | a0002 | c0009 | t0001 | g0041 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02630 | hp2 | a0002 | c0029 | t0003 | g0053 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02647 | hp1 | a0014 | c0090 | t0001 | g0124 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02647 | hp2 | a0002 | c0077 | t0001 | g0095 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02698 | hp1 | a0003 | c0002 | t0012 | g0277 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02698 | hp2 | a0007 | c0006 | t0001 | g0094 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02717 | hp2 | a0002 | c0005 | t0007 | g0057 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02723 | hp1 | a0002 | c0009 | t0003 | g0365 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02723 | hp2 | a0028 | c0043 | t0001 | g0032 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02735 | hp2 | a0009 | c0012 | t0002 | g0326 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02738 | hp1 | a0007 | c0006 | t0001 | g0153 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02738 | hp2 | a0015 | c0030 | t0001 | g0050 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02809 | hp1 | a0007 | c0072 | t0001 | g0051 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02809 | hp2 | a0002 | c0037 | t0003 | g0366 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02818 | hp1 | a0007 | c0006 | t0004 | g0008 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02886 | hp1 | a0007 | c0006 | t0001 | g0369 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02895 | hp2 | a0007 | c0006 | t0001 | g0006 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02896 | hp1 | a0001 | c0028 | t0007 | g0046 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02897 | hp1 | a0007 | c0006 | t0001 | g0007 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02897 | hp2 | a0001 | c0028 | t0007 | g0044 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02922 | hp1 | a0001 | c0042 | t0001 | g0098 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02922 | hp2 | a0002 | c0009 | t0001 | g0036 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02965 | hp1 | a0041 | c0094 | t0001 | g0308 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02965 | hp2 | a0002 | c0026 | t0003 | g0086 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02970 | hp1 | a0001 | c0016 | t0008 | g0045 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02976 | hp1 | a0001 | c0042 | t0001 | g0082 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02976 | hp2 | a0019 | c0023 | t0001 | g0170 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03041 | hp1 | a0042 | c0071 | t0004 | g0013 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03041 | hp2 | a0043 | c0093 | t0003 | g0307 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03098 | hp1 | a0002 | c0029 | t0003 | g0054 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03098 | hp2 | a0001 | c0028 | t0001 | g0364 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03130 | hp1 | a0002 | c0029 | t0001 | g0055 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03130 | hp2 | a0007 | c0006 | t0015 | g0011 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03139 | hp1 | a0044 | c0069 | t0004 | g0014 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03195 | hp1 | a0015 | c0024 | t0001 | g0161 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03195 | hp2 | a0007 | c0038 | t0001 | g0367 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03209 | hp1 | a0027 | c0039 | t0009 | g0010 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03225 | hp1 | a0045 | c0088 | t0005 | g0102 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03225 | hp2 | a0013 | c0014 | t0001 | g0077 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03239 | hp1 | a0009 | c0012 | t0002 | g0294 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03239 | hp2 | a0004 | c0019 | t0001 | g0209 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03486 | hp1 | a0015 | c0024 | t0001 | g0371 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03486 | hp2 | a0026 | c0034 | t0003 | g0167 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03490 | hp1 | a0009 | c0012 | t0002 | g0003 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03491 | hp2 | a0014 | c0017 | t0001 | g0069 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03492 | hp1 | a0014 | c0017 | t0001 | g0071 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03492 | hp2 | a0009 | c0012 | t0002 | g0003 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03516 | hp2 | a0002 | c0009 | t0013 | g0048 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03540 | hp1 | a0019 | c0023 | t0001 | g0309 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03540 | hp2 | a0046 | c0091 | t0001 | g0157 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03579 | hp1 | a0028 | c0043 | t0001 | g0033 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03579 | hp2 | a0001 | c0016 | t0001 | g0356 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03654 | hp1 | a0003 | c0002 | t0001 | g0283 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03654 | hp2 | a0001 | c0036 | t0001 | g0341 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03669 | hp1 | a0001 | c0031 | t0005 | g0063 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03669 | hp2 | a0006 | c0004 | t0001 | g0205 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03688 | hp1 | a0022 | c0027 | t0001 | g0198 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03688 | hp2 | a0007 | c0038 | t0011 | g0368 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03704 | hp1 | a0016 | c0018 | t0001 | g0275 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03704 | hp2 | a0003 | c0002 | t0001 | g0325 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03710 | hp1 | a0006 | c0004 | t0001 | g0221 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03710 | hp2 | a0047 | c0050 | t0001 | g0311 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03831 | hp1 | a0002 | c0009 | t0002 | g0358 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03831 | hp2 | a0048 | c0075 | t0001 | g0348 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03834 | hp1 | a0049 | c0084 | t0001 | g0064 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03834 | hp2 | a0008 | c0007 | t0002 | g0096 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03927 | hp1 | a0022 | c0027 | t0001 | g0218 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03927 | hp2 | a0013 | c0014 | t0001 | g0092 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0351 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03942 | hp2 | a0007 | c0079 | t0003 | g0144 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG04115 | hp1 | a0002 | c0005 | t0003 | g0149 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG04115 | hp2 | a0006 | c0004 | t0001 | g0252 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG04184 | hp1 | a0022 | c0027 | t0001 | g0222 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG04184 | hp2 | a0003 | c0002 | t0001 | g0317 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG04199 | hp1 | a0002 | c0005 | t0002 | g0346 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG04199 | hp2 | a0004 | c0008 | t0002 | g0171 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG04204 | hp1 | a0007 | c0006 | t0001 | g0120 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG04228 | hp1 | a0050 | c0064 | t0001 | g0234 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG04228 | hp2 | a0020 | c0022 | t0001 | g0269 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18522 | hp1 | a0013 | c0014 | t0001 | g0088 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18522 | hp2 | a0002 | c0026 | t0003 | g0085 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18612 | hp1 | a0020 | c0022 | t0001 | g0284 | EAS | CHB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18612 | hp2 | a0005 | c0003 | t0001 | g0178 | EAS | CHB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18906 | hp1 | a0002 | c0009 | t0001 | g0049 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18943 | hp1 | a0012 | c0013 | t0001 | g0132 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18943 | hp2 | a0005 | c0003 | t0002 | g0210 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18944 | hp1 | a0004 | c0008 | t0002 | g0199 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18944 | hp2 | a0003 | c0002 | t0001 | g0322 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18945 | hp1 | a0051 | c0046 | t0001 | g0306 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18945 | hp2 | a0003 | c0002 | t0001 | g0300 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18948 | hp1 | a0006 | c0060 | t0003 | g0233 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18948 | hp2 | a0008 | c0007 | t0002 | g0059 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18950 | hp1 | a0003 | c0002 | t0001 | g0315 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18950 | hp2 | a0008 | c0007 | t0001 | g0154 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18951 | hp1 | a0008 | c0040 | t0003 | g0146 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18951 | hp2 | a0003 | c0002 | t0001 | g0292 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18952 | hp1 | a0005 | c0003 | t0001 | g0186 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18952 | hp2 | a0008 | c0007 | t0002 | g0136 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18954 | hp1 | a0005 | c0003 | t0001 | g0179 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18956 | hp1 | a0025 | c0033 | t0001 | g0183 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18956 | hp2 | a0018 | c0020 | t0001 | g0068 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18957 | hp1 | a0002 | c0005 | t0002 | g0022 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18957 | hp2 | a0011 | c0011 | t0001 | g0197 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18962 | hp1 | a0008 | c0007 | t0002 | g0072 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18962 | hp2 | a0005 | c0003 | t0001 | g0230 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18964 | hp1 | a0005 | c0003 | t0002 | g0211 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18964 | hp2 | a0003 | c0002 | t0001 | g0295 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18966 | hp1 | a0010 | c0010 | t0001 | g0026 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18966 | hp2 | a0005 | c0059 | t0001 | g0259 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18967 | hp1 | a0016 | c0018 | t0001 | g0314 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18967 | hp2 | a0010 | c0010 | t0001 | g0140 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18968 | hp1 | a0008 | c0007 | t0002 | g0060 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18968 | hp2 | a0005 | c0003 | t0001 | g0180 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18969 | hp1 | a0003 | c0015 | t0003 | g0281 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18969 | hp2 | a0004 | c0019 | t0001 | g0223 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18970 | hp1 | a0009 | c0049 | t0001 | g0280 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18970 | hp2 | a0006 | c0004 | t0001 | g0194 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18971 | hp1 | a0014 | c0017 | t0001 | g0074 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18971 | hp2 | a0003 | c0002 | t0001 | g0286 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18973 | hp1 | a0002 | c0005 | t0002 | g0019 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18973 | hp2 | a0052 | c0086 | t0001 | g0116 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18975 | hp1 | a0011 | c0011 | t0001 | g0354 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18975 | hp2 | a0008 | c0007 | t0002 | g0139 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18977 | hp1 | a0003 | c0015 | t0003 | g0265 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18977 | hp2 | a0053 | c0092 | t0001 | g0227 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18980 | hp1 | a0009 | c0012 | t0002 | g0301 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18980 | hp2 | a0012 | c0013 | t0001 | g0131 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18981 | hp1 | a0003 | c0015 | t0003 | g0261 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18981 | hp2 | a0010 | c0010 | t0001 | g0152 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18982 | hp1 | a0018 | c0020 | t0001 | g0126 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18982 | hp2 | a0015 | c0024 | t0002 | g0021 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18983 | hp1 | a0003 | c0015 | t0003 | g0263 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18983 | hp2 | a0001 | c0087 | t0001 | g0024 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18985 | hp1 | a0010 | c0010 | t0001 | g0028 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18985 | hp2 | a0020 | c0022 | t0001 | g0298 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18986 | hp1 | a0015 | c0030 | t0001 | g0016 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18986 | hp2 | a0008 | c0007 | t0002 | g0087 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18988 | hp1 | a0003 | c0002 | t0001 | g0310 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18988 | hp2 | a0005 | c0003 | t0001 | g0203 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18989 | hp1 | a0018 | c0020 | t0001 | g0073 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18989 | hp2 | a0016 | c0018 | t0001 | g0320 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18990 | hp1 | a0008 | c0007 | t0001 | g0075 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18990 | hp2 | a0003 | c0002 | t0001 | g0285 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18991 | hp1 | a0054 | c0083 | t0001 | g0076 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18991 | hp2 | a0010 | c0010 | t0001 | g0025 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18992 | hp1 | a0023 | c0041 | t0002 | g0079 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18992 | hp2 | a0005 | c0003 | t0001 | g0258 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18993 | hp1 | a0020 | c0022 | t0001 | g0289 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18993 | hp2 | a0004 | c0008 | t0002 | g0226 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18995 | hp1 | a0010 | c0010 | t0001 | g0027 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18995 | hp2 | a0009 | c0012 | t0002 | g0319 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18998 | hp1 | a0003 | c0002 | t0001 | g0299 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18998 | hp2 | a0004 | c0008 | t0002 | g0225 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18999 | hp1 | a0007 | c0006 | t0001 | g0118 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18999 | hp2 | a0004 | c0008 | t0002 | g0229 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19000 | hp1 | a0006 | c0004 | t0002 | g0242 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19000 | hp2 | a0004 | c0008 | t0001 | g0173 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19002 | hp1 | a0006 | c0044 | t0014 | g0172 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19002 | hp2 | a0012 | c0013 | t0001 | g0138 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19004 | hp1 | a0005 | c0055 | t0001 | g0177 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19004 | hp2 | a0015 | c0030 | t0001 | g0029 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19005 | hp1 | a0006 | c0004 | t0001 | g0248 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19005 | hp2 | a0055 | c0048 | t0002 | g0262 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19006 | hp1 | a0011 | c0011 | t0001 | g0184 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19006 | hp2 | a0008 | c0007 | t0002 | g0134 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19007 | hp1 | a0003 | c0002 | t0001 | g0302 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19007 | hp2 | a0005 | c0003 | t0001 | g0254 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19009 | hp1 | a0004 | c0008 | t0002 | g0327 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19009 | hp2 | a0012 | c0013 | t0001 | g0155 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19010 | hp1 | a0005 | c0003 | t0001 | g0204 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19010 | hp2 | a0008 | c0040 | t0003 | g0135 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19030 | hp1 | a0002 | c0009 | t0001 | g0043 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19030 | hp2 | a0001 | c0080 | t0008 | g0128 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19043 | hp1 | a0013 | c0014 | t0001 | g0089 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19043 | hp2 | a0007 | c0006 | t0001 | g0370 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19054 | hp1 | a0012 | c0013 | t0001 | g0133 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19054 | hp2 | a0005 | c0003 | t0001 | g0255 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19055 | hp1 | a0003 | c0002 | t0001 | g0270 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19055 | hp2 | a0008 | c0007 | t0002 | g0129 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19056 | hp1 | a0003 | c0002 | t0001 | g0287 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19056 | hp2 | a0004 | c0008 | t0002 | g0328 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19057 | hp1 | a0007 | c0006 | t0001 | g0119 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19057 | hp2 | a0003 | c0002 | t0001 | g0321 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19060 | hp1 | a0007 | c0006 | t0001 | g0115 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19060 | hp2 | a0017 | c0025 | t0001 | g0081 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19063 | hp1 | a0016 | c0018 | t0001 | g0318 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19063 | hp2 | a0018 | c0020 | t0001 | g0147 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19065 | hp1 | a0006 | c0004 | t0001 | g0202 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19065 | hp2 | a0003 | c0002 | t0001 | g0296 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19066 | hp1 | a0004 | c0008 | t0002 | g0224 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19066 | hp2 | a0003 | c0015 | t0003 | g0267 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19068 | hp1 | a0018 | c0020 | t0001 | g0066 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19068 | hp2 | a0006 | c0004 | t0001 | g0185 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19074 | hp1 | a0009 | c0012 | t0002 | g0304 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19074 | hp2 | a0003 | c0015 | t0001 | g0264 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19076 | hp2 | a0017 | c0025 | t0001 | g0017 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19079 | hp1 | a0003 | c0002 | t0001 | g0313 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19079 | hp2 | a0056 | c0052 | t0001 | g0231 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19081 | hp1 | a0005 | c0003 | t0001 | g0200 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19081 | hp2 | a0012 | c0013 | t0001 | g0145 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19087 | hp1 | a0003 | c0002 | t0001 | g0291 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19087 | hp2 | a0008 | c0007 | t0002 | g0137 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19088 | hp1 | a0009 | c0012 | t0002 | g0288 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19088 | hp2 | a0004 | c0008 | t0001 | g0329 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19091 | hp1 | a0004 | c0008 | t0002 | g0239 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19091 | hp2 | a0003 | c0002 | t0001 | g0266 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19240 | hp1 | a0057 | c0078 | t0001 | g0164 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA19240 | hp2 | a0002 | c0009 | t0001 | g0037 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA20129 | hp1 | a0015 | c0024 | t0001 | g0162 | AFR | ASW | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA20129 | hp2 | a0004 | c0019 | t0001 | g0201 | AFR | ASW | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA20752 | hp1 | a0058 | c0062 | t0001 | g0196 | EUR | TSI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0163 | EUR | TSI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0323 | EUR | TSI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA20805 | hp2 | a0002 | c0009 | t0003 | g0359 | EUR | TSI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG01123 | hp2 | a0006 | c0004 | t0001 | g0213 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02109 | hp1 | a0036 | c0076 | t0003 | g0005 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02109 | hp2 | a0026 | c0034 | t0003 | g0168 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02486 | hp1 | a0019 | c0023 | t0001 | g0241 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02486 | hp2 | a0001 | c0016 | t0001 | g0040 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02559 | hp1 | a0013 | c0014 | t0001 | g0091 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG02559 | hp2 | a0002 | c0037 | t0003 | g0357 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03471 | hp1 | a0002 | c0009 | t0001 | g0039 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG03471 | hp2 | a0001 | c0031 | t0005 | g0330 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG06807 | hp1 | a0002 | c0009 | t0001 | g0038 | AFR | USA | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
HG06807 | hp2 | a0003 | c0002 | t0001 | g0305 | AFR | USA | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18955 | hp1 | a0017 | c0025 | t0001 | g0097 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA18955 | hp2 | a0003 | c0015 | t0001 | g0312 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA20300 | hp1 | a0002 | c0005 | t0001 | g0142 | AFR | USA | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA20300 | hp2 | a0010 | c0010 | t0001 | g0148 | AFR | USA | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
NA21309 | hp2 | a0013 | c0014 | t0001 | g0090 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
homoSapiens | chm13v2 | a0004 | c0053 | t0001 | g0208 | REF | REF | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
homoSapiens | grch38p0 | a0004 | c0032 | t0002 | g0235 | REF | REF | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:175077421 | G | T | 2 | a0041 a0043 |
2 | HG02965.hp1 HG03041.hp2 |
start_lost | HIGH | c.3G>T | p.Met1? | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 141/5042 | 3/3900 | 1/1299 | chr1 | 175077421 | |||
chr1:175077476 | C | G | 1 | a0053 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.58C>G | p.Leu20Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 196/5042 | 58/3900 | 20/1299 | chr1 | 175077476 | |||
chr1:175077653 | A | G | 30 | a0001 a0002 a0007 others(27): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
missense_variant | MODERATE | c.235A>G | p.Arg79Gly | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 373/5042 | 235/3900 | 79/1299 | chr1 | 175077653 | |||
chr1:175077690 | G | A | 2 | a0013 a0033 |
9 | HG01358.hp1 HG01891.hp2 HG01943.hp1 others(6): Show |
missense_variant | MODERATE | c.272G>A | p.Arg91His | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 410/5042 | 272/3900 | 91/1299 | chr1 | 175077690 | |||
chr1:175077699 | C | T | 1 | a0024 | 2 | HG00738.hp1 HG01993.hp1 |
missense_variant | MODERATE | c.281C>T | p.Thr94Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 419/5042 | 281/3900 | 94/1299 | chr1 | 175077699 | |||
chr1:175077784 | G | A | 1 | a0030 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.366G>A | p.Met122Ile | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 504/5042 | 366/3900 | 122/1299 | chr1 | 175077784 | |||
chr1:175077806 | C | T | 1 | a0046 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.388C>T | p.Arg130Cys | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 526/5042 | 388/3900 | 130/1299 | chr1 | 175077806 | |||
chr1:175079461 | C | T | 1 | a0041 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.538C>T | p.Arg180Cys | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/19 | 676/5042 | 538/3900 | 180/1299 | chr1 | 175079461 | |||
chr1:175079570 | T | A | 1 | a0051 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.647T>A | p.Val216Glu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/19 | 785/5042 | 647/3900 | 216/1299 | chr1 | 175079570 | |||
chr1:175080243 | G | A | 8 | a0003 a0009 a0016 others(5): Show |
61 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(58): Show |
missense_variant | MODERATE | c.865G>A | p.Asp289Asn | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/19 | 1003/5042 | 865/3900 | 289/1299 | chr1 | 175080243 | |||
chr1:175080345 | C | T | 1 | a0032 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.967C>T | p.Pro323Ser | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/19 | 1105/5042 | 967/3900 | 323/1299 | chr1 | 175080345 | |||
chr1:175080367 | C | A | 1 | a0056 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.989C>A | p.Thr330Asn | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/19 | 1127/5042 | 989/3900 | 330/1299 | chr1 | 175080367 | |||
chr1:175080386 | T | A | 1 | a0028 | 2 | HG02723.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.1008T>A | p.Asn336Lys | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/19 | 1146/5042 | 1008/3900 | 336/1299 | chr1 | 175080386 | |||
chr1:175083806 | G | A | 1 | a0028 | 2 | HG02723.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.1105G>A | p.Val369Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/19 | 1243/5042 | 1105/3900 | 369/1299 | chr1 | 175083806 | |||
chr1:175094242 | A | G | 1 | a0034 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.1577A>G | p.Asn526Ser | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/19 | 1715/5042 | 1577/3900 | 526/1299 | chr1 | 175094242 | |||
chr1:175097558 | TGGTGGGG others(905): Show |
T | 1 | a0032 | 1 | HG01261.hp1 | conservative_inframe_deletion | MODERATE | c.1755_2018del | p.Thr585_Ser672del | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/19 | 1893/5042 | 1755/3900 | 585/1299 | INFO_REALIGN_3_PRIME | chr1 | 175097558 | ||
chr1:175098538 | G | T | 1 | a0022 | 3 | HG03688.hp1 HG03927.hp1 HG04184.hp1 |
missense_variant | MODERATE | c.2062G>T | p.Val688Leu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/19 | 2200/5042 | 2062/3900 | 688/1299 | chr1 | 175098538 | |||
chr1:175117080 | C | T | 4 | a0039 a0042 a0044 others(1): Show |
4 | HG02622.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.2261C>T | p.Pro754Leu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/19 | 2399/5042 | 2261/3900 | 754/1299 | chr1 | 175117080 | |||
chr1:175118593 | T | C | 19 | a0001 a0002 a0007 others(16): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
missense_variant | MODERATE | c.2419T>C | p.Trp807Arg | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2557/5042 | 2419/3900 | 807/1299 | chr1 | 175118593 | |||
chr1:175118674 | G | A | 1 | a0048 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.2500G>A | p.Ala834Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2638/5042 | 2500/3900 | 834/1299 | chr1 | 175118674 | |||
chr1:175118710 | G | A | 2 | a0041 a0043 |
2 | HG02965.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.2536G>A | p.Glu846Lys | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2674/5042 | 2536/3900 | 846/1299 | chr1 | 175118710 | |||
chr1:175118749 | A | G | 17 | a0003 a0009 a0010 others(14): Show |
88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
missense_variant | MODERATE | c.2575A>G | p.Met859Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2713/5042 | 2575/3900 | 859/1299 | chr1 | 175118749 | |||
chr1:175123495 | A | C | 1 | a0058 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.2746A>C | p.Met916Leu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 2884/5042 | 2746/3900 | 916/1299 | chr1 | 175123495 | |||
chr1:175123538 | C | T | 34 | a0001 a0003 a0006 others(31): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
missense_variant | MODERATE | c.2789C>T | p.Pro930Leu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 2927/5042 | 2789/3900 | 930/1299 | chr1 | 175123538 | |||
chr1:175123571 | C | T | 13 | a0001 a0011 a0013 others(10): Show |
95 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(92): Show |
missense_variant | MODERATE | c.2822C>T | p.Thr941Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 2960/5042 | 2822/3900 | 941/1299 | chr1 | 175123571 | |||
chr1:175123606 | G | A | 1 | a0038 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2857G>A | p.Val953Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 2995/5042 | 2857/3900 | 953/1299 | chr1 | 175123606 | |||
chr1:175126994 | C | T | 1 | a0054 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.2954C>T | p.Thr985Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/19 | 3092/5042 | 2954/3900 | 985/1299 | chr1 | 175126994 | |||
chr1:175128129 | G | A | 1 | a0031 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.3143G>A | p.Arg1048His | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/19 | 3281/5042 | 3143/3900 | 1048/1299 | chr1 | 175128129 | |||
chr1:175128132 | G | A | 1 | a0048 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.3146G>A | p.Arg1049Gln | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/19 | 3284/5042 | 3146/3900 | 1049/1299 | chr1 | 175128132 | |||
chr1:175128727 | C | T | 2 | a0040 a0045 |
2 | HG02622.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.3311C>T | p.Thr1104Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/19 | 3449/5042 | 3311/3900 | 1104/1299 | chr1 | 175128727 | |||
chr1:175135858 | G | A | 1 | a0057 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.3344G>A | p.Arg1115Gln | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/19 | 3482/5042 | 3344/3900 | 1115/1299 | chr1 | 175135858 | |||
chr1:175135902 | G | A | 2 | a0027 a0028 |
4 | HG02451.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.3388G>A | p.Val1130Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/19 | 3526/5042 | 3388/3900 | 1130/1299 | chr1 | 175135902 | |||
chr1:175135919 | C | A | 1 | a0039 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.3405C>A | p.Asp1135Glu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/19 | 3543/5042 | 3405/3900 | 1135/1299 | chr1 | 175135919 | |||
chr1:175136860 | C | T | 10 | a0005 a0015 a0017 others(7): Show |
50 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(47): Show |
missense_variant | MODERATE | c.3467C>T | p.Ala1156Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/19 | 3605/5042 | 3467/3900 | 1156/1299 | chr1 | 175136860 | |||
chr1:175136950 | G | A | 1 | a0036 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.3557G>A | p.Arg1186Gln | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/19 | 3695/5042 | 3557/3900 | 1186/1299 | chr1 | 175136950 | |||
chr1:175146986 | T | C | 1 | a0047 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.3815T>C | p.Leu1272Ser | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 3953/5042 | 3815/3900 | 1272/1299 | chr1 | 175146986 | |||
chr1:175147034 | A | G | 1 | a0037 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.3863A>G | p.Lys1288Arg | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 4001/5042 | 3863/3900 | 1288/1299 | chr1 | 175147034 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:175077643 | G | A | 1 | a0006c0044 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.225G>A | p.Leu75Leu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 363/5042 | 225/3900 | 75/1299 | chr1 | 175077643 | |||
chr1:175079349 | C | T | 1 | a0014c0090 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.426C>T | p.Cys142Cys | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/19 | 564/5042 | 426/3900 | 142/1299 | chr1 | 175079349 | |||
chr1:175079457 | C | T | 1 | a0028c0043 | 2 | HG02723.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.534C>T | p.His178His | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/19 | 672/5042 | 534/3900 | 178/1299 | chr1 | 175079457 | |||
chr1:175079598 | G | A | 1 | a0001c0036 | 2 | HG01106.hp2 HG03654.hp2 |
synonymous_variant | LOW | c.675G>A | p.Ser225Ser | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/19 | 813/5042 | 675/3900 | 225/1299 | chr1 | 175079598 | |||
chr1:175080269 | C | A | 9 | a0001c0016 a0001c0028 a0002c0009 others(6): Show |
32 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(29): Show |
synonymous_variant | LOW | c.891C>A | p.Pro297Pro | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/19 | 1029/5042 | 891/3900 | 297/1299 | chr1 | 175080269 | |||
chr1:175083760 | G | T | 1 | a0028c0043 | 2 | HG02723.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.1059G>T | p.Val353Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/19 | 1197/5042 | 1059/3900 | 353/1299 | chr1 | 175083760 | |||
chr1:175085412 | C | T | 48 | a0001c0001 a0001c0016 a0001c0028 others(45): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
synonymous_variant | LOW | c.1242C>T | p.His414His | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/19 | 1380/5042 | 1242/3900 | 414/1299 | chr1 | 175085412 | |||
chr1:175097583 | T | C | 1 | a0050c0064 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1755T>C | p.Thr585Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/19 | 1893/5042 | 1755/3900 | 585/1299 | chr1 | 175097583 | |||
chr1:175097622 | G | A | 2 | a0003c0002 a0010c0010 |
2 | NA18971.hp2 NA18981.hp2 |
synonymous_variant | LOW | c.1794G>A | p.Val598Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/19 | 1932/5042 | 1794/3900 | 598/1299 | chr1 | 175097622 | |||
chr1:175098513 | A | G | 3 | a0001c0042 a0002c0026 a0045c0088 |
7 | HG01070.hp2 HG01071.hp1 HG02922.hp1 others(4): Show |
synonymous_variant | LOW | c.2037A>G | p.Arg679Arg | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/19 | 2175/5042 | 2037/3900 | 679/1299 | chr1 | 175098513 | |||
chr1:175098576 | C | T | 1 | a0001c0087 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.2100C>T | p.Ala700Ala | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/19 | 2238/5042 | 2100/3900 | 700/1299 | chr1 | 175098576 | |||
chr1:175117081 | G | A | 1 | a0004c0054 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.2262G>A | p.Pro754Pro | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/19 | 2400/5042 | 2262/3900 | 754/1299 | chr1 | 175117081 | |||
chr1:175117126 | G | A | 1 | a0005c0055 | 1 | NA19004.hp1 | synonymous_variant | LOW | c.2307G>A | p.Pro769Pro | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/19 | 2445/5042 | 2307/3900 | 769/1299 | chr1 | 175117126 | |||
chr1:175118634 | G | A | 1 | a0003c0047 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.2460G>A | p.Val820Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2598/5042 | 2460/3900 | 820/1299 | chr1 | 175118634 | |||
chr1:175118748 | C | T | 22 | a0003c0002 a0003c0015 a0003c0047 others(19): Show |
88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
synonymous_variant | LOW | c.2574C>T | p.Gly858Gly | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2712/5042 | 2574/3900 | 858/1299 | chr1 | 175118748 | |||
chr1:175123440 | G | A | 1 | a0049c0084 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.2691G>A | p.Thr897Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 2829/5042 | 2691/3900 | 897/1299 | chr1 | 175123440 | |||
chr1:175123647 | C | T | 1 | a0021c0058 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.2898C>T | p.Asp966Asp | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 3036/5042 | 2898/3900 | 966/1299 | chr1 | 175123647 | |||
chr1:175127022 | G | A | 4 | a0021c0056 a0021c0058 a0038c0085 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(1): Show |
synonymous_variant | LOW | c.2982G>A | p.Thr994Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/19 | 3120/5042 | 2982/3900 | 994/1299 | chr1 | 175127022 | |||
chr1:175127043 | C | T | 2 | a0001c0028 a0001c0081 |
4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.3003C>T | p.His1001His | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/19 | 3141/5042 | 3003/3900 | 1001/1299 | chr1 | 175127043 | |||
chr1:175128686 | C | T | 4 | a0027c0039 a0028c0043 a0040c0065 others(1): Show |
6 | HG02451.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
synonymous_variant | LOW | c.3270C>T | p.Gly1090Gly | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/19 | 3408/5042 | 3270/3900 | 1090/1299 | chr1 | 175128686 | |||
chr1:175128728 | G | A | 17 | a0001c0031 a0003c0015 a0004c0019 others(14): Show |
67 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(64): Show |
synonymous_variant | LOW | c.3312G>A | p.Thr1104Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/19 | 3450/5042 | 3312/3900 | 1104/1299 | chr1 | 175128728 | |||
chr1:175128731 | C | T | 2 | a0002c0037 a0009c0049 |
3 | HG02559.hp2 HG02809.hp2 NA18970.hp1 |
synonymous_variant | LOW | c.3315C>T | p.Asp1105Asp | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/19 | 3453/5042 | 3315/3900 | 1105/1299 | chr1 | 175128731 | |||
chr1:175136849 | C | T | 1 | a0001c0080 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.3456C>T | p.Thr1152Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/19 | 3594/5042 | 3456/3900 | 1152/1299 | chr1 | 175136849 | |||
chr1:175136861 | G | A | 1 | a0007c0079 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.3468G>A | p.Ala1156Ala | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/19 | 3606/5042 | 3468/3900 | 1156/1299 | chr1 | 175136861 | |||
chr1:175136864 | G | T | 1 | a0002c0077 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.3471G>T | p.Arg1157Arg | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/19 | 3609/5042 | 3471/3900 | 1157/1299 | chr1 | 175136864 | |||
chr1:175144442 | T | C | 90 | a0001c0001 a0001c0016 a0001c0028 others(87): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.3651T>C | p.Asn1217Asn | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/19 | 3789/5042 | 3651/3900 | 1217/1299 | chr1 | 175144442 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:175067873 | C | T | 1 | a0002c0005t0016 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-98C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/19 | 9546 | chr1 | 175067873 | ||||||
chr1:175067903 | C | T | 7 | a0002c0005t0004 a0007c0006t0004 a0007c0006t0015 others(4): Show |
8 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-68C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/19 | 9516 | chr1 | 175067903 | ||||||
chr1:175147116 | C | G | 104 | a0001c0001t0001 a0001c0016t0001 a0001c0016t0008 others(101): Show |
318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*45C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 45 | chr1 | 175147116 | ||||||
chr1:175147141 | T | A | 18 | a0002c0005t0003 a0002c0009t0003 a0002c0026t0003 others(15): Show |
35 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*70T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 70 | chr1 | 175147141 | ||||||
chr1:175147147 | C | G | 2 | a0001c0028t0007 a0002c0005t0007 |
3 | HG02717.hp2 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*76C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 76 | chr1 | 175147147 | ||||||
chr1:175147382 | C | A | 3 | a0001c0031t0005 a0040c0065t0010 a0045c0088t0005 |
5 | HG01884.hp1 HG02622.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*311C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 311 | chr1 | 175147382 | ||||||
chr1:175147400 | G | C | 1 | a0007c0038t0011 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*329G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 329 | chr1 | 175147400 | ||||||
chr1:175147496 | C | T | 1 | a0006c0044t0014 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*425C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 425 | chr1 | 175147496 | ||||||
chr1:175147521 | T | C | 1 | a0003c0002t0012 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*450T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 450 | chr1 | 175147521 | ||||||
chr1:175147676 | G | A | 1 | a0007c0006t0015 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 605 | chr1 | 175147676 | ||||||
chr1:175147781 | A | G | 2 | a0001c0016t0008 a0001c0080t0008 |
2 | HG02970.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*710A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 710 | chr1 | 175147781 | ||||||
chr1:175147799 | T | C | 1 | a0040c0065t0010 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*728T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 728 | chr1 | 175147799 | ||||||
chr1:175147869 | C | T | 1 | a0002c0009t0013 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*798C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 798 | chr1 | 175147869 | ||||||
chr1:175147936 | G | A | 3 | a0021c0056t0006 a0021c0058t0006 a0033c0067t0006 |
3 | HG01943.hp1 HG02145.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*865G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 865 | chr1 | 175147936 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:175068081 | G | C | 1 | a0009c0021t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-36+146G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068081 | |||||||
chr1:175068086 | A | G | 17 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(14): Show |
17 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36+151A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068086 | |||||||
chr1:175068157 | G | T | 1 | a0011c0011t0001g0354 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-36+222G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068157 | |||||||
chr1:175068538 | C | T | 1 | a0004c0019t0001g0353 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-36+603C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068538 | |||||||
chr1:175068559 | C | T | 23 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0333 others(20): Show |
23 | HG00099.hp2 HG01106.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.-36+624C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068559 | |||||||
chr1:175068634 | T | C | 206 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-36+699T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068634 | |||||||
chr1:175068662 | T | G | 1 | a0001c0016t0001g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-36+727T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068662 | |||||||
chr1:175068856 | C | T | 3 | a0026c0034t0003g0167 a0026c0034t0003g0168 a0040c0065t0010g0166 |
3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-36+921C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068856 | |||||||
chr1:175069162 | A | G | 3 | a0004c0008t0001g0329 a0004c0008t0002g0327 a0004c0008t0002g0328 |
3 | NA19009.hp1 NA19056.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-36+1227A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069162 | |||||||
chr1:175069212 | A | G | 274 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-36+1277A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069212 | |||||||
chr1:175069222 | C | T | 2 | a0001c0001t0001g0165 a0057c0078t0001g0164 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-36+1287C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069222 | |||||||
chr1:175069235 | G | A | 93 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(90): Show |
93 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(90): Show |
intron_variant | MODIFIER | c.-36+1300G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069235 | |||||||
chr1:175069323 | T | C | 7 | a0003c0002t0001g0266 a0003c0015t0001g0264 a0003c0015t0003g0261 others(4): Show |
7 | NA18977.hp1 NA18981.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.-36+1388T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069323 | |||||||
chr1:175069586 | T | C | 3 | a0007c0006t0001g0006 a0007c0006t0001g0007 a0036c0076t0003g0005 |
3 | HG02109.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-36+1651T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069586 | |||||||
chr1:175069699 | A | G | 206 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-36+1764A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069699 | |||||||
chr1:175069735 | A | G | 1 | a0009c0012t0002g0326 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-36+1800A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069735 | |||||||
chr1:175069871 | A | C | 1 | a0001c0001t0002g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-36+1936A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069871 | |||||||
chr1:175069878 | C | A | 1 | a0013c0014t0001g0056 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-36+1943C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069878 | |||||||
chr1:175069919 | A | T | 1 | a0003c0002t0001g0325 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-36+1984A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069919 | |||||||
chr1:175070161 | A | G | 5 | a0001c0073t0001g0052 a0002c0029t0001g0055 a0002c0029t0003g0053 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+2226A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070161 | |||||||
chr1:175070464 | C | T | 1 | a0015c0030t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-36+2529C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070464 | |||||||
chr1:175070467 | T | C | 50 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(47): Show |
50 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.-36+2532T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070467 | |||||||
chr1:175070627 | C | T | 2 | a0015c0024t0001g0161 a0015c0024t0001g0162 |
2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-36+2692C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070627 | |||||||
chr1:175070890 | G | A | 1 | a0035c0063t0001g0268 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-36+2955G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070890 | |||||||
chr1:175070912 | C | T | 206 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-36+2977C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070912 | |||||||
chr1:175071729 | G | T | 3 | a0007c0006t0001g0369 a0007c0006t0001g0370 a0015c0024t0001g0371 |
3 | HG02886.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-36+3794G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175071729 | |||||||
chr1:175071771 | T | C | 1 | a0001c0001t0002g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-36+3836T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175071771 | |||||||
chr1:175071805 | G | A | 3 | a0026c0034t0003g0167 a0026c0034t0003g0168 a0040c0065t0010g0166 |
3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-36+3870G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175071805 | |||||||
chr1:175072016 | C | A | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36+4081C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072016 | |||||||
chr1:175072030 | G | T | 5 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0031t0005g0156 others(2): Show |
5 | HG01192.hp2 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+4095G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072030 | |||||||
chr1:175072250 | C | A | 1 | a0031c0068t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-36+4315C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072250 | |||||||
chr1:175072391 | G | A | 7 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0333 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+4456G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072391 | |||||||
chr1:175072413 | A | G | 110 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(107): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-36+4478A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072413 | |||||||
chr1:175072437 | A | T | 40 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(37): Show |
40 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.-36+4502A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072437 | |||||||
chr1:175072558 | G | C | 1 | a0001c0031t0005g0330 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-36+4623G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072558 | |||||||
chr1:175072682 | T | C | 1 | a0005c0003t0001g0169 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-35-4702T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072682 | |||||||
chr1:175072841 | G | T | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-4543G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072841 | |||||||
chr1:175072910 | T | C | 93 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(90): Show |
93 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(90): Show |
intron_variant | MODIFIER | c.-35-4474T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072910 | |||||||
chr1:175072917 | A | G | 1 | a0007c0038t0011g0368 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-35-4467A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072917 | |||||||
chr1:175072926 | C | CT | 48 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(45): Show |
48 | HG00438.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.-35-4434dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175072926 | ||||||
chr1:175072926 | CT | C | 138 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-35-4434delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175072926 | ||||||
chr1:175072926 | CTTTTTTT others(4): Show |
C | 3 | a0007c0006t0001g0369 a0007c0006t0001g0370 a0015c0024t0001g0371 |
3 | HG02886.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35-4444_-35-4434d others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175072926 | ||||||
chr1:175073020 | C | G | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-4364C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073020 | |||||||
chr1:175073069 | C | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-35-4315C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073069 | |||||||
chr1:175073172 | T | C | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-4212T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073172 | |||||||
chr1:175073309 | C | T | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-4075C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073309 | |||||||
chr1:175073318 | T | G | 1 | a0020c0022t0001g0269 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-35-4066T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073318 | |||||||
chr1:175073577 | C | T | 1 | a0007c0006t0001g0153 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-35-3807C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073577 | |||||||
chr1:175073690 | C | T | 115 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(112): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-35-3694C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073690 | |||||||
chr1:175073876 | C | T | 2 | a0015c0024t0001g0161 a0015c0024t0001g0162 |
2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-35-3508C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073876 | |||||||
chr1:175073924 | A | AGCTCGGG others(14): Show |
11 | a0001c0016t0001g0040 a0002c0009t0001g0036 a0002c0009t0001g0037 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-35-3459_-35-3439d others(23): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175073924 | ||||||
chr1:175074023 | T | C | 1 | a0014c0017t0001g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-35-3361T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074023 | |||||||
chr1:175074062 | G | A | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-3322G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074062 | |||||||
chr1:175074107 | A | G | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-3277A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074107 | |||||||
chr1:175074273 | A | G | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-3111A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074273 | |||||||
chr1:175074421 | A | T | 3 | a0001c0001t0001g0125 a0010c0010t0001g0152 a0018c0020t0001g0126 |
3 | NA18981.hp2 NA18982.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-35-2963A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074421 | |||||||
chr1:175074484 | G | GA | 63 | a0003c0002t0001g0266 a0003c0002t0001g0278 a0003c0002t0001g0279 others(60): Show |
64 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-35-2875dupA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175074484 | ||||||
chr1:175074484 | G | GAA | 6 | a0003c0002t0001g0270 a0003c0002t0001g0313 a0003c0002t0001g0315 others(3): Show |
6 | NA18950.hp1 NA18955.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35-2876_-35-2875d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175074484 | ||||||
chr1:175074484 | GAAAAAAA others(2): Show |
G | 47 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(44): Show |
47 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.-35-2883_-35-2875d others(11): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175074484 | ||||||
chr1:175074484 | GAAAAAAA others(3): Show |
G | 160 | a0001c0001t0001g0031 a0001c0001t0001g0062 a0001c0001t0001g0093 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-35-2884_-35-2875d others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175074484 | ||||||
chr1:175074484 | GAAAAAAA others(4): Show |
G | 1 | a0014c0090t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-35-2885_-35-2875d others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175074484 | ||||||
chr1:175074543 | G | T | 5 | a0004c0008t0002g0239 a0004c0019t0002g0237 a0006c0004t0002g0242 others(2): Show |
5 | HG00408.hp1 HG02040.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-2841G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074543 | |||||||
chr1:175074754 | T | C | 2 | a0041c0094t0001g0308 a0043c0093t0003g0307 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-35-2630T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074754 | |||||||
chr1:175074819 | T | C | 11 | a0004c0008t0003g0246 a0004c0008t0003g0247 a0004c0019t0001g0353 others(8): Show |
11 | HG01069.hp2 HG01071.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-2565T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074819 | |||||||
chr1:175074831 | C | T | 9 | a0001c0073t0001g0052 a0002c0029t0001g0055 a0002c0029t0003g0053 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-35-2553C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074831 | |||||||
chr1:175074929 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0151 |
2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-35-2455C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074929 | |||||||
chr1:175074943 | C | G | 3 | a0026c0034t0003g0167 a0026c0034t0003g0168 a0040c0065t0010g0166 |
3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-35-2441C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074943 | |||||||
chr1:175075321 | C | T | 3 | a0039c0070t0004g0015 a0042c0071t0004g0013 a0044c0069t0004g0014 |
3 | HG02622.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-35-2063C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075321 | |||||||
chr1:175075418 | T | C | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.-35-1966T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075418 | |||||||
chr1:175075546 | A | G | 66 | a0003c0002t0001g0266 a0003c0002t0001g0270 a0003c0002t0001g0278 others(63): Show |
67 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-35-1838A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075546 | |||||||
chr1:175075546 | A | T | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-1838A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075546 | |||||||
chr1:175075664 | T | C | 93 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(90): Show |
93 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(90): Show |
intron_variant | MODIFIER | c.-35-1720T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075664 | |||||||
chr1:175075694 | T | C | 93 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(90): Show |
93 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(90): Show |
intron_variant | MODIFIER | c.-35-1690T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075694 | |||||||
chr1:175075870 | A | G | 1 | a0051c0046t0001g0306 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-35-1514A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075870 | |||||||
chr1:175075878 | G | A | 93 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(90): Show |
93 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(90): Show |
intron_variant | MODIFIER | c.-35-1506G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075878 | |||||||
chr1:175076080 | A | T | 91 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(88): Show |
91 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(88): Show |
intron_variant | MODIFIER | c.-35-1304A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076080 | |||||||
chr1:175076158 | A | T | 3 | a0026c0034t0003g0167 a0026c0034t0003g0168 a0040c0065t0010g0166 |
3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-35-1226A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076158 | |||||||
chr1:175076198 | A | T | 44 | a0001c0001t0001g0165 a0001c0016t0001g0040 a0001c0016t0001g0355 others(41): Show |
44 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.-35-1186A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076198 | |||||||
chr1:175076223 | G | A | 1 | a0014c0090t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-35-1161G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076223 | |||||||
chr1:175076350 | C | A | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-1034C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076350 | |||||||
chr1:175076632 | T | G | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-752T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076632 | |||||||
chr1:175076704 | G | A | 12 | a0001c0001t0001g0165 a0002c0005t0004g0009 a0007c0006t0001g0369 others(9): Show |
12 | HG01891.hp1 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35-680G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076704 | |||||||
chr1:175076749 | C | G | 31 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0123 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-35-635C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076749 | |||||||
chr1:175076766 | G | C | 115 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(112): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-35-618G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076766 | |||||||
chr1:175076936 | T | C | 3 | a0026c0034t0003g0167 a0026c0034t0003g0168 a0040c0065t0010g0166 |
3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-35-448T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076936 | |||||||
chr1:175077318 | T | TAA | 32 | a0001c0016t0001g0040 a0001c0016t0001g0355 a0001c0016t0001g0356 others(29): Show |
32 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.-35-58_-35-57dupAA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175077318 | ||||||
chr1:175077341 | A | G | 10 | a0001c0001t0001g0165 a0002c0005t0004g0009 a0007c0006t0001g0369 others(7): Show |
10 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-43A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175077341 | |||||||
chr1:175077352 | G | A | 205 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-35-32G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175077352 | |||||||
chr1:175077971 | T | G | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.409+144T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175077971 | |||||||
chr1:175077983 | A | G | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.409+156A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175077983 | |||||||
chr1:175078104 | C | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.409+277C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078104 | |||||||
chr1:175078164 | T | C | 1 | a0006c0004t0001g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.409+337T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078164 | |||||||
chr1:175078220 | C | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.409+393C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078220 | |||||||
chr1:175078223 | T | C | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.409+396T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078223 | |||||||
chr1:175078236 | A | G | 1 | a0018c0020t0001g0147 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.409+409A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078236 | |||||||
chr1:175078246 | T | C | 62 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(59): Show |
62 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.409+419T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078246 | |||||||
chr1:175078440 | C | T | 3 | a0039c0070t0004g0015 a0042c0071t0004g0013 a0044c0069t0004g0014 |
3 | HG02622.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.409+613C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078440 | |||||||
chr1:175078453 | G | A | 3 | a0009c0012t0003g0273 a0009c0021t0001g0271 a0009c0021t0001g0272 |
3 | HG01109.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.409+626G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078453 | |||||||
chr1:175078581 | C | T | 1 | a0045c0088t0005g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.410-752C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078581 | |||||||
chr1:175078618 | C | T | 1 | a0002c0029t0001g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.410-715C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078618 | |||||||
chr1:175078656 | G | C | 91 | a0004c0008t0001g0173 a0004c0008t0001g0228 a0004c0008t0001g0329 others(88): Show |
91 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.410-677G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078656 | |||||||
chr1:175078664 | A | G | 62 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(59): Show |
62 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.410-669A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078664 | |||||||
chr1:175078757 | G | A | 1 | a0005c0003t0001g0176 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.410-576G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078757 | |||||||
chr1:175078917 | T | C | 2 | a0001c0001t0001g0331 a0038c0085t0001g0335 |
2 | HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.410-416T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078917 | |||||||
chr1:175079008 | G | T | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.410-325G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175079008 | |||||||
chr1:175079028 | G | A | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.410-305G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175079028 | |||||||
chr1:175079815 | C | G | 1 | a0012c0013t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.784+108C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/18 | chr1 | 175079815 | |||||||
chr1:175079873 | G | T | 5 | a0001c0001t0001g0123 a0001c0001t0001g0151 a0001c0001t0002g0122 others(2): Show |
5 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+166G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/18 | chr1 | 175079873 | |||||||
chr1:175079880 | T | C | 1 | a0038c0085t0001g0335 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.784+173T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/18 | chr1 | 175079880 | |||||||
chr1:175079967 | A | AGT | 212 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.785-180_785-179dup others(2): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 175079967 | ||||||
chr1:175079967 | A | AGTGT | 4 | a0010c0010t0001g0025 a0010c0010t0001g0026 a0010c0010t0001g0027 others(1): Show |
4 | NA18966.hp1 NA18985.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.785-182_785-179dup others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 175079967 | ||||||
chr1:175080448 | C | T | 1 | a0003c0002t0001g0322 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1048+22C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080448 | |||||||
chr1:175080460 | G | C | 1 | a0002c0005t0001g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1048+34G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080460 | |||||||
chr1:175080499 | C | T | 2 | a0001c0001t0001g0350 a0048c0075t0001g0348 |
2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1048+73C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080499 | |||||||
chr1:175080731 | T | G | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1048+305T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080731 | |||||||
chr1:175080752 | A | C | 1 | a0019c0023t0001g0241 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048+326A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080752 | |||||||
chr1:175080755 | G | A | 4 | a0002c0005t0003g0104 a0002c0005t0003g0105 a0002c0005t0003g0106 others(1): Show |
4 | HG01192.hp1 HG01943.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048+329G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080755 | |||||||
chr1:175080814 | C | G | 202 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(199): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1048+388C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080814 | |||||||
chr1:175081046 | C | G | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1048+620C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081046 | |||||||
chr1:175081098 | C | A | 3 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 |
3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1048+672C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081098 | |||||||
chr1:175081297 | C | T | 1 | a0050c0064t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1048+871C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081297 | |||||||
chr1:175081343 | C | T | 1 | a0033c0067t0006g0100 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1048+917C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081343 | |||||||
chr1:175081423 | C | A | 202 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(199): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1048+997C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081423 | |||||||
chr1:175081699 | G | A | 1 | a0005c0055t0001g0177 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1048+1273G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081699 | |||||||
chr1:175081733 | A | G | 1 | a0002c0005t0003g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1048+1307A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081733 | |||||||
chr1:175081742 | GACCATAG others(4): Show |
G | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1048+1318_1048+132 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 175081742 | ||||||
chr1:175081747 | T | C | 6 | a0001c0001t0001g0338 a0001c0001t0001g0352 a0001c0036t0001g0341 others(3): Show |
6 | HG00099.hp2 HG01106.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048+1321T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081747 | |||||||
chr1:175081766 | C | G | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1048+1340C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081766 | |||||||
chr1:175081816 | G | C | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1048+1390G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081816 | |||||||
chr1:175081889 | A | C | 1 | a0002c0005t0001g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1048+1463A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081889 | |||||||
chr1:175082215 | T | G | 3 | a0019c0023t0001g0309 a0021c0056t0006g0274 a0021c0058t0006g0316 |
3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1049-1535T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082215 | |||||||
chr1:175082391 | T | C | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1049-1359T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082391 | |||||||
chr1:175082396 | G | A | 2 | a0009c0012t0002g0326 a0016c0018t0001g0275 |
2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1049-1354G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082396 | |||||||
chr1:175082448 | C | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1049-1302C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082448 | |||||||
chr1:175082501 | A | C | 1 | a0002c0005t0003g0106 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1049-1249A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082501 | |||||||
chr1:175082707 | A | G | 274 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1049-1043A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082707 | |||||||
chr1:175082983 | G | GT | 52 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(49): Show |
52 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1049-754dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 175082983 | ||||||
chr1:175083084 | T | C | 2 | a0005c0003t0001g0178 a0005c0003t0001g0179 |
2 | NA18612.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1049-666T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083084 | |||||||
chr1:175083254 | G | A | 200 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1049-496G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083254 | |||||||
chr1:175083273 | C | A | 1 | a0005c0003t0001g0180 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1049-477C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083273 | |||||||
chr1:175083489 | G | A | 2 | a0005c0003t0001g0181 a0006c0004t0001g0182 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1049-261G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083489 | |||||||
chr1:175083518 | G | GA | 3 | a0019c0023t0001g0309 a0021c0056t0006g0274 a0021c0058t0006g0316 |
3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1049-232_1049-231i others(3): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083518 | |||||||
chr1:175083520 | G | A | 3 | a0019c0023t0001g0309 a0021c0056t0006g0274 a0021c0058t0006g0316 |
3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1049-230G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083520 | |||||||
chr1:175083692 | G | A | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1049-58G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083692 | |||||||
chr1:175083962 | T | C | 43 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(40): Show |
43 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.1234+27T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175083962 | |||||||
chr1:175083965 | A | T | 202 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(199): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1234+30A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175083965 | |||||||
chr1:175084252 | A | G | 1 | a0008c0007t0002g0099 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1234+317A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084252 | |||||||
chr1:175084301 | C | A | 6 | a0007c0006t0001g0006 a0007c0006t0001g0007 a0026c0034t0003g0167 others(3): Show |
6 | HG02109.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234+366C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084301 | |||||||
chr1:175084438 | C | T | 1 | a0013c0014t0001g0056 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1234+503C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084438 | |||||||
chr1:175084484 | A | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1234+549A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084484 | |||||||
chr1:175084550 | C | T | 2 | a0001c0001t0001g0352 a0002c0005t0002g0347 |
2 | HG01361.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1234+615C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084550 | |||||||
chr1:175084562 | T | C | 1 | a0031c0068t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1234+627T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084562 | |||||||
chr1:175084581 | C | T | 1 | a0014c0090t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1234+646C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084581 | |||||||
chr1:175084713 | T | A | 3 | a0026c0034t0003g0167 a0026c0034t0003g0168 a0040c0065t0010g0166 |
3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1235-692T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084713 | |||||||
chr1:175084792 | G | T | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1235-613G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084792 | |||||||
chr1:175084886 | A | G | 6 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1235-519A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084886 | |||||||
chr1:175085233 | C | T | 1 | a0005c0003t0001g0232 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1235-172C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175085233 | |||||||
chr1:175085282 | A | G | 205 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1235-123A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175085282 | |||||||
chr1:175085321 | C | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1235-84C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175085321 | |||||||
chr1:175085353 | G | C | 5 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1235-52G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175085353 | |||||||
chr1:175085643 | G | A | 2 | a0041c0094t0001g0308 a0043c0093t0003g0307 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1324+149G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175085643 | |||||||
chr1:175085644 | G | A | 11 | a0001c0016t0001g0040 a0002c0009t0001g0036 a0002c0009t0001g0037 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1324+150G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175085644 | |||||||
chr1:175085828 | C | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1324+334C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175085828 | |||||||
chr1:175085874 | C | CA | 8 | a0001c0042t0001g0098 a0002c0005t0003g0149 a0007c0006t0001g0006 others(5): Show |
8 | HG01358.hp2 HG02895.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324+400dupA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175085874 | ||||||
chr1:175085874 | C | CAA | 113 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0123 others(110): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1324+399_1324+400d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175085874 | ||||||
chr1:175085874 | C | CAAA | 77 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(74): Show |
77 | HG00099.hp2 HG00438.hp1 HG01074.hp2 others(74): Show |
intron_variant | MODIFIER | c.1324+398_1324+400d others(5): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175085874 | ||||||
chr1:175086086 | C | A | 200 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+592C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086086 | |||||||
chr1:175086418 | C | A | 45 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(42): Show |
45 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1324+924C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086418 | |||||||
chr1:175086420 | A | G | 1 | a0056c0052t0001g0231 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1324+926A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086420 | |||||||
chr1:175086512 | C | T | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1324+1018C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086512 | |||||||
chr1:175086514 | T | C | 274 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1324+1020T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086514 | |||||||
chr1:175086517 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1324+1023G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086517 | |||||||
chr1:175086572 | G | A | 1 | a0015c0030t0001g0016 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1324+1078G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086572 | |||||||
chr1:175086783 | T | C | 3 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 |
3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1324+1289T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086783 | |||||||
chr1:175086815 | T | C | 200 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+1321T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086815 | |||||||
chr1:175087027 | C | T | 1 | a0009c0012t0002g0304 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1324+1533C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087027 | |||||||
chr1:175087029 | G | C | 202 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(199): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1324+1535G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087029 | |||||||
chr1:175087070 | A | C | 1 | a0014c0090t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1324+1576A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087070 | |||||||
chr1:175087078 | A | C | 1 | a0006c0004t0002g0242 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1324+1584A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087078 | |||||||
chr1:175087104 | A | C | 1 | a0050c0064t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1324+1610A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087104 | |||||||
chr1:175087167 | C | T | 1 | a0008c0007t0002g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1324+1673C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087167 | |||||||
chr1:175087215 | C | A | 200 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+1721C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087215 | |||||||
chr1:175087380 | G | A | 202 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(199): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1324+1886G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087380 | |||||||
chr1:175087418 | C | T | 45 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(42): Show |
45 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1324+1924C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087418 | |||||||
chr1:175087421 | C | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1324+1927C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087421 | |||||||
chr1:175087733 | T | A | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1324+2239T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087733 | |||||||
chr1:175087797 | A | G | 198 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1324+2303A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087797 | |||||||
chr1:175087807 | C | A | 55 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(52): Show |
55 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.1324+2313C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087807 | |||||||
chr1:175087852 | C | T | 2 | a0005c0003t0001g0230 a0005c0003t0001g0232 |
2 | HG02132.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1324+2358C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087852 | |||||||
chr1:175087867 | C | A | 44 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(41): Show |
44 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.1324+2373C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087867 | |||||||
chr1:175087882 | G | A | 32 | a0001c0016t0001g0040 a0001c0016t0001g0355 a0001c0016t0001g0356 others(29): Show |
32 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1324+2388G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087882 | |||||||
chr1:175087895 | C | T | 3 | a0002c0029t0001g0055 a0002c0029t0003g0053 a0002c0029t0003g0054 |
3 | HG02630.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1324+2401C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087895 | |||||||
chr1:175087896 | G | A | 1 | a0008c0007t0002g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1324+2402G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087896 | |||||||
chr1:175087922 | C | A | 1 | a0006c0004t0002g0242 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1324+2428C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087922 | |||||||
chr1:175088056 | C | A | 3 | a0026c0034t0003g0167 a0026c0034t0003g0168 a0040c0065t0010g0166 |
3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1324+2562C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088056 | |||||||
chr1:175088112 | G | A | 14 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(11): Show |
14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.1324+2618G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088112 | |||||||
chr1:175088185 | C | T | 1 | a0050c0064t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1324+2691C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088185 | |||||||
chr1:175088187 | C | A | 44 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(41): Show |
44 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.1324+2693C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088187 | |||||||
chr1:175088195 | G | C | 3 | a0039c0070t0004g0015 a0042c0071t0004g0013 a0044c0069t0004g0014 |
3 | HG02622.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1324+2701G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088195 | |||||||
chr1:175088195 | G | T | 44 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(41): Show |
44 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.1324+2701G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088195 | |||||||
chr1:175088240 | T | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1324+2746T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088240 | |||||||
chr1:175088437 | C | A | 199 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(196): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1324+2943C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088437 | |||||||
chr1:175088547 | G | A | 110 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(107): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1324+3053G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088547 | |||||||
chr1:175088618 | A | G | 1 | a0002c0077t0001g0095 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1324+3124A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088618 | |||||||
chr1:175088626 | T | C | 200 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+3132T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088626 | |||||||
chr1:175088646 | A | G | 199 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(196): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1324+3152A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088646 | |||||||
chr1:175088763 | A | G | 6 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+3269A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088763 | |||||||
chr1:175088814 | T | G | 200 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+3320T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088814 | |||||||
chr1:175088986 | C | T | 200 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+3492C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088986 | |||||||
chr1:175089035 | A | AC | 12 | a0004c0008t0001g0173 a0004c0008t0001g0228 a0004c0008t0001g0329 others(9): Show |
12 | HG02015.hp2 NA18966.hp2 NA18968.hp2 others(9): Show |
intron_variant | MODIFIER | c.1324+3543dupC | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175089035 | ||||||
chr1:175089284 | C | T | 2 | a0001c0001t0001g0165 a0057c0078t0001g0164 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1324+3790C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089284 | |||||||
chr1:175089326 | A | C | 39 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(36): Show |
39 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1324+3832A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089326 | |||||||
chr1:175089390 | G | A | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1324+3896G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089390 | |||||||
chr1:175089535 | T | G | 6 | a0010c0010t0001g0110 a0010c0010t0001g0111 a0010c0010t0001g0112 others(3): Show |
6 | HG01243.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1324+4041T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089535 | |||||||
chr1:175089610 | T | C | 2 | a0009c0021t0001g0271 a0009c0021t0001g0272 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1324+4116T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089610 | |||||||
chr1:175089951 | G | C | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-4039G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089951 | |||||||
chr1:175090147 | C | T | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3843C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090147 | |||||||
chr1:175090179 | G | T | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-3811G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090179 | |||||||
chr1:175090330 | C | G | 1 | a0031c0068t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1325-3660C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090330 | |||||||
chr1:175090337 | T | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3653T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090337 | |||||||
chr1:175090397 | T | C | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-3593T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090397 | |||||||
chr1:175090414 | G | T | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3576G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090414 | |||||||
chr1:175090418 | C | G | 6 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-3572C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090418 | |||||||
chr1:175090445 | C | T | 6 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-3545C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090445 | |||||||
chr1:175090447 | GC | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3537delC | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175090447 | ||||||
chr1:175090500 | C | T | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3490C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090500 | |||||||
chr1:175090501 | A | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3489A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090501 | |||||||
chr1:175090502 | G | A | 2 | a0041c0094t0001g0308 a0043c0093t0003g0307 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1325-3488G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090502 | |||||||
chr1:175090546 | T | C | 14 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(11): Show |
14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.1325-3444T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090546 | |||||||
chr1:175090604 | A | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3386A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090604 | |||||||
chr1:175090610 | C | T | 1 | a0005c0055t0001g0177 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1325-3380C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090610 | |||||||
chr1:175090628 | G | C | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3362G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090628 | |||||||
chr1:175090656 | T | C | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3334T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090656 | |||||||
chr1:175090657 | G | A | 3 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 |
3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1325-3333G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090657 | |||||||
chr1:175090706 | G | A | 2 | a0011c0011t0001g0184 a0011c0011t0001g0354 |
2 | NA18975.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1325-3284G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090706 | |||||||
chr1:175090749 | AATTAG | A | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-3238_1325-323 others(9): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175090749 | ||||||
chr1:175090841 | T | C | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3149T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090841 | |||||||
chr1:175090851 | A | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3139A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090851 | |||||||
chr1:175090852 | T | C | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-3138T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090852 | |||||||
chr1:175091017 | T | C | 268 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(265): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1325-2973T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091017 | |||||||
chr1:175091147 | C | T | 1 | a0003c0002t0001g0303 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1325-2843C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091147 | |||||||
chr1:175091205 | A | G | 1 | a0008c0007t0002g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1325-2785A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091205 | |||||||
chr1:175091370 | G | T | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-2620G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091370 | |||||||
chr1:175091428 | C | T | 275 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(272): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1325-2562C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091428 | |||||||
chr1:175091546 | T | TTTTA | 40 | a0001c0001t0001g0093 a0001c0001t0001g0123 a0001c0001t0001g0141 others(37): Show |
41 | HG00544.hp2 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1325-2437_1325-243 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091546 | ||||||
chr1:175091555 | TTA | T | 46 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(43): Show |
46 | HG00099.hp1 HG00438.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.1325-2433_1325-243 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091555 | ||||||
chr1:175091557 | A | T | 114 | a0001c0001t0001g0062 a0001c0001t0001g0107 a0001c0001t0001g0108 others(111): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1325-2433A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091557 | |||||||
chr1:175091558 | T | A | 113 | a0001c0001t0001g0062 a0001c0001t0001g0107 a0001c0001t0001g0108 others(110): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-2432T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091558 | |||||||
chr1:175091559 | T | A | 1 | a0002c0005t0007g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325-2431T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091559 | |||||||
chr1:175091559 | T | TTTTA | 34 | a0001c0042t0001g0082 a0002c0029t0003g0053 a0002c0029t0003g0054 others(31): Show |
34 | HG00280.hp1 HG00438.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1325-2387_1325-238 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091559 | ||||||
chr1:175091559 | T | TTTTATTT others(1): Show |
4 | a0006c0004t0001g0185 a0006c0004t0001g0243 a0006c0004t0001g0244 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-2391_1325-238 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091559 | ||||||
chr1:175091559 | TTTTA | T | 15 | a0003c0002t0001g0302 a0003c0002t0001g0305 a0005c0003t0001g0230 others(12): Show |
15 | HG00639.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1325-2387_1325-238 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091559 | ||||||
chr1:175091559 | TTTTATTT others(21): Show |
T | 1 | a0004c0019t0001g0223 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1325-2411_1325-238 others(32): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091559 | ||||||
chr1:175091560 | T | A | 46 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(43): Show |
46 | HG00099.hp1 HG00438.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.1325-2430T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091560 | |||||||
chr1:175091561 | T | A | 113 | a0001c0001t0001g0062 a0001c0001t0001g0107 a0001c0001t0001g0108 others(110): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-2429T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091561 | |||||||
chr1:175091562 | T | A | 1 | a0002c0005t0007g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325-2428T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091562 | |||||||
chr1:175091563 | A | T | 114 | a0001c0001t0001g0062 a0001c0001t0001g0107 a0001c0001t0001g0108 others(111): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1325-2427A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091563 | |||||||
chr1:175091565 | TTA | T | 39 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(36): Show |
39 | HG00099.hp1 HG00438.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1325-2423_1325-242 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091565 | ||||||
chr1:175091565 | TTATTTA | T | 7 | a0002c0077t0001g0095 a0007c0006t0001g0094 a0007c0006t0001g0153 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-2423_1325-241 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091565 | ||||||
chr1:175091658 | A | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-2332A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091658 | |||||||
chr1:175091665 | T | C | 39 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(36): Show |
39 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1325-2325T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091665 | |||||||
chr1:175091683 | G | A | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-2307G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091683 | |||||||
chr1:175091780 | C | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-2210C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091780 | |||||||
chr1:175091781 | G | A | 1 | a0001c0016t0001g0360 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1325-2209G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091781 | |||||||
chr1:175091793 | T | A | 1 | a0017c0074t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1325-2197T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091793 | |||||||
chr1:175091810 | G | A | 2 | a0008c0007t0002g0059 a0008c0007t0002g0060 |
2 | NA18948.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1325-2180G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091810 | |||||||
chr1:175091814 | T | C | 1 | a0025c0033t0001g0236 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1325-2176T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091814 | |||||||
chr1:175091825 | A | G | 1 | a0008c0007t0002g0099 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1325-2165A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091825 | |||||||
chr1:175091922 | C | T | 32 | a0001c0016t0001g0040 a0001c0016t0001g0355 a0001c0016t0001g0356 others(29): Show |
32 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1325-2068C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091922 | |||||||
chr1:175091950 | G | A | 10 | a0001c0001t0001g0165 a0002c0005t0004g0009 a0007c0006t0001g0369 others(7): Show |
10 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1325-2040G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091950 | |||||||
chr1:175092092 | G | T | 1 | a0005c0003t0001g0258 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1325-1898G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092092 | |||||||
chr1:175092103 | C | T | 1 | a0006c0061t0002g0217 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1325-1887C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092103 | |||||||
chr1:175092236 | T | A | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-1754T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092236 | |||||||
chr1:175092269 | C | T | 87 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(84): Show |
87 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(84): Show |
intron_variant | MODIFIER | c.1325-1721C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092269 | |||||||
chr1:175092295 | C | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-1695C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092295 | |||||||
chr1:175092394 | C | CAGACTAT others(4): Show |
201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-1587_1325-158 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175092394 | ||||||
chr1:175092451 | G | C | 1 | a0003c0002t0001g0317 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1325-1539G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092451 | |||||||
chr1:175092467 | G | A | 1 | a0044c0069t0004g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1325-1523G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092467 | |||||||
chr1:175092479 | C | G | 1 | a0001c0001t0001g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1325-1511C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092479 | |||||||
chr1:175092523 | C | A | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-1467C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092523 | |||||||
chr1:175092542 | C | A | 32 | a0001c0016t0001g0040 a0001c0016t0001g0355 a0001c0016t0001g0356 others(29): Show |
32 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1325-1448C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092542 | |||||||
chr1:175092798 | G | A | 6 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-1192G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092798 | |||||||
chr1:175092802 | C | A | 197 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1325-1188C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092802 | |||||||
chr1:175092935 | T | A | 1 | a0011c0011t0003g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1325-1055T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092935 | |||||||
chr1:175092967 | T | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-1023T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092967 | |||||||
chr1:175092973 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1325-1017C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092973 | |||||||
chr1:175093056 | C | T | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-934C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093056 | |||||||
chr1:175093103 | A | G | 1 | a0002c0009t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1325-887A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093103 | |||||||
chr1:175093243 | C | A | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1325-747C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093243 | |||||||
chr1:175093243 | C | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1325-747C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093243 | |||||||
chr1:175093364 | G | T | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-626G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093364 | |||||||
chr1:175093402 | T | C | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-588T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093402 | |||||||
chr1:175093410 | T | G | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-580T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093410 | |||||||
chr1:175093421 | A | G | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-569A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093421 | |||||||
chr1:175093528 | A | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-462A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093528 | |||||||
chr1:175093555 | C | T | 201 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-435C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093555 | |||||||
chr1:175093563 | CTG | C | 10 | a0001c0001t0001g0165 a0002c0005t0004g0009 a0007c0006t0001g0369 others(7): Show |
10 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1325-424_1325-423d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175093563 | ||||||
chr1:175093582 | A | G | 3 | a0011c0011t0001g0215 a0024c0035t0001g0214 a0024c0035t0001g0216 |
3 | HG00280.hp2 HG00738.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1325-408A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093582 | |||||||
chr1:175093829 | C | T | 1 | a0037c0051t0001g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1325-161C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093829 | |||||||
chr1:175093858 | G | A | 1 | a0013c0014t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1325-132G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093858 | |||||||
chr1:175094358 | A | G | 1 | a0007c0038t0001g0367 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1588+105A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094358 | |||||||
chr1:175094435 | A | G | 45 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(42): Show |
45 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1588+182A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094435 | |||||||
chr1:175094500 | C | A | 3 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 |
3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1588+247C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094500 | |||||||
chr1:175094538 | T | G | 1 | a0012c0013t0001g0061 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1588+285T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094538 | |||||||
chr1:175094543 | T | C | 1 | a0009c0012t0002g0326 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1588+290T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094543 | |||||||
chr1:175094569 | C | T | 1 | a0002c0009t0003g0359 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1588+316C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094569 | |||||||
chr1:175094723 | G | C | 16 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0141 others(13): Show |
16 | HG01192.hp2 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1588+470G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094723 | |||||||
chr1:175094734 | C | T | 1 | a0002c0009t0002g0358 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1588+481C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094734 | |||||||
chr1:175094762 | G | A | 3 | a0026c0034t0003g0167 a0026c0034t0003g0168 a0040c0065t0010g0166 |
3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1588+509G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094762 | |||||||
chr1:175094887 | C | T | 2 | a0005c0003t0001g0178 a0005c0003t0001g0179 |
2 | NA18612.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1588+634C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094887 | |||||||
chr1:175094905 | G | A | 6 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1588+652G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094905 | |||||||
chr1:175095100 | A | G | 1 | a0002c0005t0003g0106 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1588+847A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095100 | |||||||
chr1:175095225 | C | T | 125 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(122): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1588+972C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095225 | |||||||
chr1:175095403 | G | A | 1 | a0011c0011t0001g0190 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1588+1150G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095403 | |||||||
chr1:175095490 | T | C | 157 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(154): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1588+1237T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095490 | |||||||
chr1:175095494 | A | G | 1 | a0011c0011t0003g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1588+1241A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095494 | |||||||
chr1:175095517 | T | G | 38 | a0001c0001t0001g0165 a0001c0016t0001g0040 a0001c0016t0001g0355 others(35): Show |
38 | HG01081.hp1 HG01168.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.1588+1264T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095517 | |||||||
chr1:175095617 | A | G | 157 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(154): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1588+1364A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095617 | |||||||
chr1:175095635 | G | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1588+1382G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095635 | |||||||
chr1:175095664 | C | T | 6 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1588+1411C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095664 | |||||||
chr1:175095854 | C | T | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1589-1563C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095854 | |||||||
chr1:175095871 | G | A | 1 | a0003c0002t0001g0302 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1589-1546G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095871 | |||||||
chr1:175095917 | CTTTTCTT others(6): Show |
C | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589-1498_1589-148 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr1 | 175095917 | ||||||
chr1:175096266 | G | A | 3 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 |
3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1589-1151G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096266 | |||||||
chr1:175096384 | A | G | 45 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(42): Show |
45 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1589-1033A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096384 | |||||||
chr1:175096388 | T | G | 2 | a0001c0001t0001g0343 a0001c0001t0001g0351 |
2 | HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1589-1029T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096388 | |||||||
chr1:175096483 | C | T | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1589-934C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096483 | |||||||
chr1:175096801 | C | T | 6 | a0010c0010t0001g0078 a0010c0010t0001g0140 a0017c0025t0001g0081 others(3): Show |
6 | HG00408.hp2 HG00609.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589-616C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096801 | |||||||
chr1:175096831 | G | A | 1 | a0031c0068t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1589-586G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096831 | |||||||
chr1:175096937 | G | C | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1589-480G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096937 | |||||||
chr1:175096972 | A | T | 5 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589-445A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096972 | |||||||
chr1:175096974 | A | G | 2 | a0007c0006t0001g0006 a0007c0006t0001g0007 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1589-443A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096974 | |||||||
chr1:175097078 | G | A | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1589-339G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175097078 | |||||||
chr1:175097170 | C | T | 10 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0028t0001g0364 others(7): Show |
10 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1589-247C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175097170 | |||||||
chr1:175097223 | T | G | 1 | a0004c0008t0002g0171 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1589-194T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175097223 | |||||||
chr1:175097831 | G | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0151 a0001c0001t0002g0122 others(2): Show |
5 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1855+148G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/18 | chr1 | 175097831 | |||||||
chr1:175097985 | T | C | 1 | a0026c0034t0003g0168 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1855+302T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/18 | chr1 | 175097985 | |||||||
chr1:175098001 | C | G | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1855+318C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/18 | chr1 | 175098001 | |||||||
chr1:175098043 | G | C | 1 | a0001c0001t0001g0343 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1856-289G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/18 | chr1 | 175098043 | |||||||
chr1:175098092 | G | A | 1 | a0001c0016t0001g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1856-240G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/18 | chr1 | 175098092 | |||||||
chr1:175098719 | TAC | T | 6 | a0007c0006t0001g0006 a0007c0006t0001g0007 a0026c0034t0003g0167 others(3): Show |
6 | HG02109.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2119+126_2119+127d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175098719 | ||||||
chr1:175098875 | T | A | 197 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2119+280T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175098875 | |||||||
chr1:175099070 | A | T | 1 | a0031c0068t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2119+475A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099070 | |||||||
chr1:175099175 | T | C | 2 | a0041c0094t0001g0308 a0043c0093t0003g0307 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2119+580T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099175 | |||||||
chr1:175099417 | G | A | 112 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.2119+822G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099417 | |||||||
chr1:175099461 | A | C | 42 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(39): Show |
42 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.2119+866A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099461 | |||||||
chr1:175099570 | AGAGGAGA others(39): Show |
A | 45 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(42): Show |
45 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.2119+984_2119+1029 others(49): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175099570 | ||||||
chr1:175099586 | C | CTCAGGAG others(16): Show |
6 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2119+1047_2119+106 others(27): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175099586 | ||||||
chr1:175099586 | CTCAGGAG others(16): Show |
C | 128 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(125): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2119+1047_2119+106 others(27): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175099586 | ||||||
chr1:175099588 | CAGG | C | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119+1002_2119+100 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175099588 | ||||||
chr1:175099629 | G | A | 1 | a0052c0086t0001g0116 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2119+1034G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099629 | |||||||
chr1:175099855 | G | A | 1 | a0011c0011t0001g0354 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2119+1260G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099855 | |||||||
chr1:175099929 | G | A | 5 | a0003c0002t0001g0283 a0003c0002t0001g0317 a0003c0002t0012g0277 others(2): Show |
5 | HG02698.hp1 HG02735.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119+1334G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099929 | |||||||
chr1:175099938 | T | C | 3 | a0019c0023t0001g0309 a0021c0056t0006g0274 a0021c0058t0006g0316 |
3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+1343T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099938 | |||||||
chr1:175099964 | A | G | 3 | a0019c0023t0001g0309 a0021c0056t0006g0274 a0021c0058t0006g0316 |
3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+1369A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099964 | |||||||
chr1:175099986 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2119+1391G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099986 | |||||||
chr1:175100234 | T | A | 25 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0123 others(22): Show |
25 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.2119+1639T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100234 | |||||||
chr1:175100287 | C | T | 12 | a0001c0016t0001g0040 a0002c0009t0001g0036 a0002c0009t0001g0037 others(9): Show |
12 | HG01081.hp1 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2119+1692C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100287 | |||||||
chr1:175100372 | A | T | 9 | a0013c0014t0001g0056 a0013c0014t0001g0077 a0013c0014t0001g0083 others(6): Show |
9 | HG01358.hp1 HG01891.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2119+1777A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100372 | |||||||
chr1:175100414 | G | C | 1 | a0014c0090t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2119+1819G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100414 | |||||||
chr1:175100433 | C | T | 1 | a0014c0090t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2119+1838C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100433 | |||||||
chr1:175100661 | C | T | 1 | a0006c0004t0001g0213 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2119+2066C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100661 | |||||||
chr1:175100669 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2119+2074G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100669 | |||||||
chr1:175100672 | A | G | 5 | a0005c0003t0001g0212 a0005c0003t0001g0257 a0005c0003t0002g0210 others(2): Show |
5 | HG01255.hp2 HG01361.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119+2077A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100672 | |||||||
chr1:175100700 | GT | G | 164 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(161): Show |
166 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2119+2116delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175100700 | ||||||
chr1:175100700 | GTT | G | 61 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2119+2115_2119+211 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175100700 | ||||||
chr1:175100757 | A | G | 68 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(65): Show |
69 | HG00099.hp2 HG00438.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.2119+2162A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100757 | |||||||
chr1:175100783 | TCAA | T | 3 | a0019c0023t0001g0309 a0021c0056t0006g0274 a0021c0058t0006g0316 |
3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+2192_2119+219 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175100783 | ||||||
chr1:175100849 | T | C | 2 | a0027c0039t0009g0010 a0027c0039t0009g0012 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2119+2254T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100849 | |||||||
chr1:175100878 | A | G | 14 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(11): Show |
14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2119+2283A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100878 | |||||||
chr1:175100953 | A | C | 1 | a0003c0002t0001g0300 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2119+2358A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100953 | |||||||
chr1:175100998 | T | TGCAAACC others(3438): Show |
1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2403_2119+240 others(3449): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100998 | |||||||
chr1:175101003 | T | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2408T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101003 | |||||||
chr1:175101004 | T | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2409T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101004 | |||||||
chr1:175101005 | A | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2410A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101005 | |||||||
chr1:175101007 | A | C | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2412A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101007 | |||||||
chr1:175101009 | A | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2414A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101009 | |||||||
chr1:175101011 | A | T | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2416A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101011 | |||||||
chr1:175101018 | A | T | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2423A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101018 | |||||||
chr1:175101023 | C | T | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2428C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101023 | |||||||
chr1:175101025 | C | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2430C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101025 | |||||||
chr1:175101026 | T | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2431T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101026 | |||||||
chr1:175101027 | T | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2432T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101027 | |||||||
chr1:175101029 | T | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2434T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101029 | |||||||
chr1:175101031 | G | T | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2436G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101031 | |||||||
chr1:175101034 | A | T | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2439A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101034 | |||||||
chr1:175101039 | G | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2444G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101039 | |||||||
chr1:175101042 | A | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2447A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101042 | |||||||
chr1:175101046 | A | C | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2451A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101046 | |||||||
chr1:175101049 | A | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2454A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101049 | |||||||
chr1:175101054 | T | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2459T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101054 | |||||||
chr1:175101057 | T | C | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2462T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101057 | |||||||
chr1:175101060 | T | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2465T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101060 | |||||||
chr1:175101064 | C | CAAGCCGT others(2577): Show |
1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2469_2119+247 others(2588): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101064 | |||||||
chr1:175101065 | T | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2470T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101065 | |||||||
chr1:175101068 | A | C | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2473A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101068 | |||||||
chr1:175101070 | T | C | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2475T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101070 | |||||||
chr1:175101073 | T | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2478T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101073 | |||||||
chr1:175101074 | C | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2479C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101074 | |||||||
chr1:175101075 | C | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2480C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101075 | |||||||
chr1:175101082 | C | T | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2487C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101082 | |||||||
chr1:175101118 | A | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2523A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101118 | |||||||
chr1:175101126 | T | C | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2531T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101126 | |||||||
chr1:175101129 | G | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2534G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101129 | |||||||
chr1:175101130 | G | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2535G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101130 | |||||||
chr1:175101138 | C | T | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2543C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101138 | |||||||
chr1:175101186 | G | C | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2591G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101186 | |||||||
chr1:175101204 | C | T | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2609C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101204 | |||||||
chr1:175101236 | T | TTGCTGGC others(117): Show |
1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2641_2119+264 others(128): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101236 | |||||||
chr1:175101237 | C | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2642C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101237 | |||||||
chr1:175101250 | A | C | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2655A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101250 | |||||||
chr1:175101275 | G | A | 1 | a0037c0051t0001g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2119+2680G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101275 | |||||||
chr1:175101276 | C | T | 2 | a0001c0087t0001g0024 a0021c0057t0001g0175 |
2 | HG01069.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2119+2681C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101276 | |||||||
chr1:175101304 | G | A | 3 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 |
3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2119+2709G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101304 | |||||||
chr1:175101305 | C | T | 1 | a0011c0011t0001g0184 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2119+2710C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101305 | |||||||
chr1:175101319 | G | C | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2724G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101319 | |||||||
chr1:175101329 | G | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2734G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101329 | |||||||
chr1:175101338 | G | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2743G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101338 | |||||||
chr1:175101345 | C | T | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2750C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101345 | |||||||
chr1:175101378 | C | T | 1 | a0011c0011t0003g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2119+2783C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101378 | |||||||
chr1:175101379 | G | GGTGA | 88 | a0003c0002t0001g0266 a0003c0002t0001g0270 a0003c0002t0001g0278 others(85): Show |
89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.2119+2787_2119+278 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175101379 | ||||||
chr1:175101434 | T | C | 14 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(11): Show |
14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2119+2839T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101434 | |||||||
chr1:175101446 | C | T | 3 | a0026c0034t0003g0167 a0026c0034t0003g0168 a0040c0065t0010g0166 |
3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2119+2851C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101446 | |||||||
chr1:175101482 | C | G | 1 | a0004c0019t0001g0209 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2119+2887C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101482 | |||||||
chr1:175101483 | G | A | 2 | a0003c0002t0001g0278 a0009c0021t0001g0276 |
2 | HG00280.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2119+2888G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101483 | |||||||
chr1:175101524 | G | C | 232 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2119+2929G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101524 | |||||||
chr1:175101529 | T | G | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2119+2934T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101529 | |||||||
chr1:175101600 | G | A | 10 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(7): Show |
10 | HG02145.hp1 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2119+3005G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101600 | |||||||
chr1:175101714 | G | A | 1 | a0025c0033t0001g0183 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2119+3119G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101714 | |||||||
chr1:175101765 | G | T | 46 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(43): Show |
46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2119+3170G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101765 | |||||||
chr1:175101812 | A | G | 3 | a0006c0004t0001g0185 a0011c0011t0001g0184 a0011c0011t0001g0354 |
3 | NA18975.hp1 NA19006.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2119+3217A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101812 | |||||||
chr1:175101812 | ACCAGAGC others(6151): Show |
A | 89 | a0003c0002t0001g0266 a0003c0002t0001g0270 a0003c0002t0001g0278 others(86): Show |
90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.2119+3330_2120-885 others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175101812 | ||||||
chr1:175101925 | A | G | 59 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(56): Show |
59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+3330A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101925 | |||||||
chr1:175101932 | A | T | 59 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(56): Show |
59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+3337A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101932 | |||||||
chr1:175101959 | C | T | 1 | a0007c0006t0004g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2119+3364C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101959 | |||||||
chr1:175101966 | G | A | 4 | a0001c0042t0001g0082 a0002c0026t0001g0002 a0002c0026t0003g0085 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2119+3371G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101966 | |||||||
chr1:175102075 | A | G | 1 | a0002c0009t0002g0358 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2119+3480A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102075 | |||||||
chr1:175102216 | CT | C | 3 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 |
3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2119+3622delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102216 | |||||||
chr1:175102287 | G | A | 1 | a0006c0004t0001g0253 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2119+3692G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102287 | |||||||
chr1:175102288 | C | T | 1 | a0005c0003t0001g0255 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2119+3693C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102288 | |||||||
chr1:175102324 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2119+3729G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102324 | |||||||
chr1:175102420 | G | A | 5 | a0001c0016t0001g0360 a0001c0016t0001g0362 a0002c0009t0002g0358 others(2): Show |
5 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2119+3825G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102420 | |||||||
chr1:175102432 | C | T | 59 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(56): Show |
59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+3837C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102432 | |||||||
chr1:175102491 | G | C | 14 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2119+3896G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102491 | |||||||
chr1:175102620 | C | A | 1 | a0001c0080t0008g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2119+4025C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102620 | |||||||
chr1:175102642 | G | A | 1 | a0002c0009t0001g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2119+4047G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102642 | |||||||
chr1:175102649 | C | A | 3 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 |
3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2119+4054C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102649 | |||||||
chr1:175102662 | T | C | 147 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2119+4067T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102662 | |||||||
chr1:175102687 | C | A | 1 | a0001c0001t0001g0352 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2119+4092C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102687 | |||||||
chr1:175102725 | T | C | 14 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2119+4130T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102725 | |||||||
chr1:175102740 | G | A | 2 | a0019c0023t0001g0309 a0021c0056t0006g0274 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+4145G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102740 | |||||||
chr1:175102764 | A | G | 147 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2119+4169A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102764 | |||||||
chr1:175102880 | C | T | 3 | a0019c0023t0001g0309 a0021c0056t0006g0274 a0021c0058t0006g0316 |
3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+4285C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102880 | |||||||
chr1:175102988 | A | G | 1 | a0001c0073t0001g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2119+4393A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102988 | |||||||
chr1:175103156 | G | A | 39 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(36): Show |
39 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.2119+4561G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103156 | |||||||
chr1:175103248 | G | A | 1 | a0008c0007t0002g0136 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2119+4653G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103248 | |||||||
chr1:175103492 | A | C | 59 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(56): Show |
59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+4897A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103492 | |||||||
chr1:175103565 | G | GCTGTTTT others(3648): Show |
1 | a0002c0029t0001g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2119+4984_2119+498 others(3659): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175103565 | ||||||
chr1:175103565 | G | GCTGTTTT others(3599): Show |
2 | a0002c0029t0003g0053 a0002c0029t0003g0054 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2119+4984_2119+498 others(3610): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175103565 | ||||||
chr1:175103637 | T | C | 1 | a0055c0048t0002g0262 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2119+5042T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103637 | |||||||
chr1:175103641 | C | T | 1 | a0019c0023t0001g0241 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2119+5046C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103641 | |||||||
chr1:175103653 | C | A | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119+5058C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103653 | |||||||
chr1:175103696 | T | C | 3 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 |
3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2119+5101T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103696 | |||||||
chr1:175103812 | C | T | 4 | a0002c0029t0001g0055 a0002c0029t0003g0053 a0002c0029t0003g0054 others(1): Show |
4 | HG01257.hp2 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2119+5217C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103812 | |||||||
chr1:175103912 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2119+5317G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103912 | |||||||
chr1:175104222 | A | G | 1 | a0031c0068t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2119+5627A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104222 | |||||||
chr1:175104231 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2119+5636G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104231 | |||||||
chr1:175104391 | A | G | 73 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(70): Show |
73 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(70): Show |
intron_variant | MODIFIER | c.2119+5796A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104391 | |||||||
chr1:175104666 | G | T | 1 | a0004c0008t0002g0199 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2119+6071G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104666 | |||||||
chr1:175104670 | C | T | 2 | a0002c0005t0007g0057 a0002c0077t0001g0095 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2119+6075C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104670 | |||||||
chr1:175104764 | A | G | 1 | a0007c0006t0004g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2119+6169A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104764 | |||||||
chr1:175104961 | G | A | 3 | a0019c0023t0001g0309 a0021c0056t0006g0274 a0021c0058t0006g0316 |
3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+6366G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104961 | |||||||
chr1:175105012 | G | A | 2 | a0002c0005t0007g0057 a0002c0077t0001g0095 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2119+6417G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105012 | |||||||
chr1:175105072 | C | T | 1 | a0008c0007t0002g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2119+6477C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105072 | |||||||
chr1:175105303 | G | A | 3 | a0002c0005t0001g0114 a0002c0005t0003g0149 a0002c0005t0003g0150 |
3 | HG00140.hp1 HG02257.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2119+6708G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105303 | |||||||
chr1:175105350 | C | T | 3 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 |
3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2119+6755C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105350 | |||||||
chr1:175105527 | G | A | 2 | a0001c0042t0001g0098 a0045c0088t0005g0102 |
2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2119+6932G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105527 | |||||||
chr1:175105641 | G | A | 14 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(11): Show |
14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2119+7046G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105641 | |||||||
chr1:175105669 | A | C | 3 | a0007c0006t0001g0369 a0007c0006t0001g0370 a0015c0024t0001g0371 |
3 | HG02886.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2119+7074A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105669 | |||||||
chr1:175105686 | G | A | 1 | a0006c0004t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2119+7091G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105686 | |||||||
chr1:175105820 | A | G | 144 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.2119+7225A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105820 | |||||||
chr1:175105881 | T | C | 5 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0031t0005g0156 others(2): Show |
5 | HG01192.hp2 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2119+7286T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105881 | |||||||
chr1:175106029 | G | C | 1 | a0007c0006t0001g0120 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2119+7434G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106029 | |||||||
chr1:175106043 | G | A | 14 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2119+7448G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106043 | |||||||
chr1:175106073 | G | A | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2119+7478G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106073 | |||||||
chr1:175106141 | G | A | 1 | a0001c0031t0005g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2119+7546G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106141 | |||||||
chr1:175106150 | T | C | 59 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(56): Show |
59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+7555T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106150 | |||||||
chr1:175106168 | C | T | 3 | a0007c0006t0001g0006 a0007c0006t0001g0007 a0036c0076t0003g0005 |
3 | HG02109.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2119+7573C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106168 | |||||||
chr1:175106215 | A | T | 3 | a0005c0003t0001g0187 a0006c0004t0001g0185 a0006c0004t0001g0253 |
3 | HG00438.hp2 HG02155.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2119+7620A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106215 | |||||||
chr1:175106257 | A | C | 5 | a0001c0016t0001g0360 a0001c0016t0001g0362 a0002c0009t0002g0358 others(2): Show |
5 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2119+7662A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106257 | |||||||
chr1:175106277 | G | A | 60 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2119+7682G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106277 | |||||||
chr1:175106356 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2119+7761A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106356 | |||||||
chr1:175106478 | C | T | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119+7883C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106478 | |||||||
chr1:175106514 | A | T | 14 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2119+7919A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106514 | |||||||
chr1:175106623 | G | T | 59 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(56): Show |
59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+8028G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106623 | |||||||
chr1:175106690 | G | A | 56 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(53): Show |
56 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.2119+8095G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106690 | |||||||
chr1:175106740 | G | C | 11 | a0001c0042t0001g0082 a0001c0042t0001g0098 a0002c0005t0007g0057 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2119+8145G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106740 | |||||||
chr1:175106742 | C | T | 3 | a0019c0023t0001g0170 a0019c0023t0001g0174 a0019c0023t0001g0241 |
3 | HG02486.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2119+8147C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106742 | |||||||
chr1:175106758 | C | T | 14 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(11): Show |
14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2119+8163C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106758 | |||||||
chr1:175106835 | C | T | 1 | a0002c0009t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2119+8240C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106835 | |||||||
chr1:175106918 | G | A | 1 | a0007c0006t0001g0369 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2119+8323G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106918 | |||||||
chr1:175106950 | G | A | 1 | a0001c0016t0001g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2119+8355G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106950 | |||||||
chr1:175106992 | G | A | 1 | a0005c0003t0001g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2119+8397G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106992 | |||||||
chr1:175107028 | C | T | 16 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(13): Show |
17 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2119+8433C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107028 | |||||||
chr1:175107066 | C | T | 4 | a0002c0005t0003g0104 a0002c0005t0003g0105 a0002c0005t0003g0106 others(1): Show |
4 | HG01192.hp1 HG01943.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2119+8471C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107066 | |||||||
chr1:175107080 | C | T | 1 | a0008c0007t0002g0130 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2119+8485C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107080 | |||||||
chr1:175107092 | C | T | 13 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0141 others(10): Show |
13 | HG01192.hp2 HG01884.hp1 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.2119+8497C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107092 | |||||||
chr1:175107112 | C | T | 60 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2119+8517C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107112 | |||||||
chr1:175107164 | C | CTCGTGGT others(124): Show |
1 | a0002c0005t0004g0009 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2119+8630_2119+876 others(135): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175107164 | ||||||
chr1:175107164 | CTCGTGGT others(124): Show |
C | 2 | a0005c0003t0001g0212 a0005c0003t0001g0257 |
2 | HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2119+8630_2119+876 others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175107164 | ||||||
chr1:175107167 | G | A | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2119+8572G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107167 | |||||||
chr1:175107288 | G | A | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2119+8693G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107288 | |||||||
chr1:175107298 | G | A | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+8703G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107298 | |||||||
chr1:175107301 | G | T | 1 | a0026c0034t0003g0168 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2119+8706G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107301 | |||||||
chr1:175107325 | G | A | 1 | a0007c0006t0001g0153 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2119+8730G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107325 | |||||||
chr1:175107327 | G | A | 14 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2119+8732G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107327 | |||||||
chr1:175107344 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2119+8749C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107344 | |||||||
chr1:175107394 | G | T | 11 | a0001c0016t0001g0040 a0002c0009t0001g0036 a0002c0009t0001g0037 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119+8799G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107394 | |||||||
chr1:175107458 | A | G | 147 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2119+8863A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107458 | |||||||
chr1:175107474 | G | A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0158 a0001c0001t0001g0160 others(3): Show |
6 | HG01192.hp2 HG01884.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2119+8879G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107474 | |||||||
chr1:175107475 | T | A | 2 | a0001c0001t0001g0165 a0057c0078t0001g0164 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2119+8880T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107475 | |||||||
chr1:175107492 | A | G | 59 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(56): Show |
59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+8897A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107492 | |||||||
chr1:175107499 | T | C | 14 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(11): Show |
14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2119+8904T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107499 | |||||||
chr1:175107561 | G | A | 1 | a0048c0075t0001g0348 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2119+8966G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107561 | |||||||
chr1:175107646 | G | T | 1 | a0001c0001t0001g0336 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2119+9051G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107646 | |||||||
chr1:175107682 | G | C | 143 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.2119+9087G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107682 | |||||||
chr1:175107687 | T | G | 59 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(56): Show |
59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+9092T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107687 | |||||||
chr1:175107745 | C | T | 2 | a0011c0011t0001g0184 a0011c0011t0001g0354 |
2 | NA18975.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2119+9150C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107745 | |||||||
chr1:175107934 | A | G | 1 | a0002c0009t0003g0359 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2120-9005A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107934 | |||||||
chr1:175107970 | G | A | 147 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2120-8969G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107970 | |||||||
chr1:175108048 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2120-8891T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108048 | |||||||
chr1:175108077 | C | CGATTGAT others(6151): Show |
1 | a0002c0005t0002g0117 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2120-8857_2120-885 others(6162): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175108077 | ||||||
chr1:175108077 | C | T | 59 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(56): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.2120-8862C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108077 | |||||||
chr1:175108080 | T | C | 1 | a0017c0074t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2120-8859T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108080 | |||||||
chr1:175108131 | C | T | 1 | a0007c0006t0001g0120 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2120-8808C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108131 | |||||||
chr1:175108148 | G | A | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-8791G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108148 | |||||||
chr1:175108148 | G | GGAGTGTT others(112): Show |
1 | a0012c0013t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2120-8755_2120-863 others(123): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175108148 | ||||||
chr1:175108151 | G | C | 1 | a0007c0006t0001g0120 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2120-8788G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108151 | |||||||
chr1:175108155 | T | C | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-8784T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108155 | |||||||
chr1:175108194 | G | C | 1 | a0006c0004t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2120-8745G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108194 | |||||||
chr1:175108233 | G | A | 19 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(16): Show |
20 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2120-8706G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108233 | |||||||
chr1:175108233 | G | C | 87 | a0003c0002t0001g0266 a0003c0002t0001g0270 a0003c0002t0001g0278 others(84): Show |
88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2120-8706G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108233 | |||||||
chr1:175108324 | T | C | 14 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(11): Show |
14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2120-8615T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108324 | |||||||
chr1:175108334 | C | T | 5 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-8605C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108334 | |||||||
chr1:175108397 | G | C | 236 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2120-8542G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108397 | |||||||
chr1:175108463 | G | C | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8476G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108463 | |||||||
chr1:175108481 | G | A | 1 | a0028c0043t0001g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2120-8458G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108481 | |||||||
chr1:175108494 | G | A | 1 | a0003c0015t0003g0265 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2120-8445G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108494 | |||||||
chr1:175108520 | T | C | 14 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2120-8419T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108520 | |||||||
chr1:175108531 | G | A | 1 | a0004c0019t0001g0209 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2120-8408G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108531 | |||||||
chr1:175108538 | A | G | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8401A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108538 | |||||||
chr1:175108539 | C | G | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2120-8400C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108539 | |||||||
chr1:175108549 | C | T | 2 | a0019c0023t0001g0170 a0019c0023t0001g0174 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2120-8390C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108549 | |||||||
chr1:175108577 | G | A | 9 | a0013c0014t0001g0056 a0013c0014t0001g0077 a0013c0014t0001g0083 others(6): Show |
9 | HG01358.hp1 HG01891.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2120-8362G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108577 | |||||||
chr1:175108594 | C | T | 1 | a0002c0009t0001g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2120-8345C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108594 | |||||||
chr1:175108722 | G | A | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8217G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108722 | |||||||
chr1:175108799 | G | A | 7 | a0001c0016t0001g0356 a0001c0028t0001g0364 a0002c0009t0003g0361 others(4): Show |
7 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2120-8140G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108799 | |||||||
chr1:175108811 | T | C | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8128T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108811 | |||||||
chr1:175108819 | T | C | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8120T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108819 | |||||||
chr1:175108827 | G | A | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8112G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108827 | |||||||
chr1:175108831 | A | G | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8108A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108831 | |||||||
chr1:175108833 | G | A | 1 | a0002c0009t0002g0358 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2120-8106G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108833 | |||||||
chr1:175108906 | A | C | 1 | a0001c0001t0001g0352 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2120-8033A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108906 | |||||||
chr1:175108946 | A | G | 3 | a0002c0029t0001g0055 a0002c0029t0003g0053 a0002c0029t0003g0054 |
3 | HG02630.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2120-7993A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108946 | |||||||
chr1:175109008 | C | T | 5 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-7931C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109008 | |||||||
chr1:175109072 | A | AT | 24 | a0002c0005t0004g0009 a0003c0002t0001g0310 a0003c0002t0001g0313 others(21): Show |
24 | HG01255.hp2 HG01361.hp2 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.2120-7840dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATT | 61 | a0003c0002t0001g0266 a0003c0002t0001g0278 a0003c0002t0001g0279 others(58): Show |
62 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.2120-7841_2120-784 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTT | 9 | a0003c0002t0001g0303 a0003c0002t0001g0322 a0003c0015t0003g0265 others(6): Show |
9 | HG00609.hp1 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2120-7842_2120-784 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(1): Show |
14 | a0001c0001t0001g0107 a0002c0005t0002g0117 a0002c0005t0003g0105 others(11): Show |
14 | HG01069.hp1 HG01192.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.2120-7847_2120-784 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(2): Show |
12 | a0001c0016t0001g0040 a0001c0073t0001g0052 a0002c0009t0001g0039 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2120-7848_2120-784 others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(3): Show |
3 | a0019c0023t0001g0309 a0021c0056t0006g0274 a0021c0058t0006g0316 |
3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2120-7849_2120-784 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(4): Show |
4 | a0015c0024t0001g0161 a0015c0024t0001g0162 a0019c0023t0001g0170 others(1): Show |
4 | HG02615.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2120-7850_2120-784 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(5): Show |
7 | a0001c0001t0001g0062 a0001c0001t0001g0338 a0001c0001t0001g0339 others(4): Show |
7 | HG01346.hp2 HG02486.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2120-7851_2120-784 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(6): Show |
24 | a0001c0001t0001g0020 a0001c0001t0001g0093 a0001c0001t0001g0141 others(21): Show |
24 | HG00099.hp2 HG01106.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.2120-7852_2120-784 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(7): Show |
12 | a0001c0001t0001g0023 a0001c0001t0001g0331 a0001c0001t0001g0351 others(9): Show |
12 | HG01167.hp1 HG01358.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.2120-7853_2120-784 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(8): Show |
3 | a0001c0001t0001g0031 a0001c0001t0001g0336 a0015c0030t0001g0050 |
3 | HG02300.hp2 HG02738.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2120-7854_2120-784 others(19): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0332 a0002c0005t0002g0347 |
2 | HG02135.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2120-7855_2120-784 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(10): Show |
2 | a0001c0001t0001g0160 a0001c0001t0001g0334 |
2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2120-7856_2120-784 others(21): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(11): Show |
1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2120-7857_2120-784 others(22): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(12): Show |
4 | a0007c0006t0001g0006 a0007c0006t0001g0115 a0007c0006t0001g0118 others(1): Show |
4 | HG02738.hp1 HG02895.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.2120-7858_2120-784 others(23): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(13): Show |
2 | a0007c0006t0001g0007 a0007c0006t0001g0119 |
2 | HG02897.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.2120-7859_2120-784 others(24): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(14): Show |
1 | a0002c0005t0016g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2120-7860_2120-784 others(25): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(17): Show |
1 | a0002c0005t0003g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2120-7863_2120-784 others(28): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(18): Show |
3 | a0001c0001t0001g0123 a0001c0001t0001g0323 a0002c0005t0001g0121 |
3 | HG00323.hp2 HG01081.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2120-7864_2120-784 others(29): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(19): Show |
1 | a0001c0001t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2120-7865_2120-784 others(30): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(20): Show |
3 | a0001c0001t0001g0324 a0001c0001t0002g0122 a0001c0001t0002g0163 |
3 | HG00099.hp1 HG01123.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2120-7866_2120-784 others(31): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(21): Show |
1 | a0001c0001t0001g0108 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2120-7840_2120-783 others(32): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(22): Show |
2 | a0002c0005t0003g0150 a0007c0006t0001g0120 |
2 | HG02257.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2120-7840_2120-783 others(33): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | A | ATTTTTTT others(23): Show |
1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2120-7840_2120-783 others(34): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | AT | A | 6 | a0001c0031t0005g0063 a0004c0008t0002g0239 a0005c0003t0001g0181 others(3): Show |
6 | HG01258.hp2 HG03041.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.2120-7840delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | ATTTTTTT others(2): Show |
A | 13 | a0001c0016t0001g0356 a0001c0016t0001g0360 a0001c0016t0001g0362 others(10): Show |
13 | HG01081.hp1 HG01261.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.2120-7848_2120-784 others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | ATTTTTTT others(3): Show |
A | 2 | a0001c0016t0001g0355 a0002c0009t0002g0363 |
2 | HG01168.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2120-7849_2120-784 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109072 | ATTTTTTT others(7): Show |
A | 14 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2120-7853_2120-784 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | ||||||
chr1:175109121 | G | A | 1 | a0015c0030t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2120-7818G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109121 | |||||||
chr1:175109130 | G | A | 60 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2120-7809G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109130 | |||||||
chr1:175109136 | C | T | 1 | a0021c0057t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2120-7803C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109136 | |||||||
chr1:175109149 | C | T | 3 | a0039c0070t0004g0015 a0042c0071t0004g0013 a0044c0069t0004g0014 |
3 | HG02622.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2120-7790C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109149 | |||||||
chr1:175109234 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2120-7705G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109234 | |||||||
chr1:175109238 | G | A | 5 | a0002c0005t0007g0057 a0002c0077t0001g0095 a0026c0034t0003g0167 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-7701G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109238 | |||||||
chr1:175109243 | C | T | 2 | a0002c0005t0007g0057 a0002c0077t0001g0095 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2120-7696C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109243 | |||||||
chr1:175109245 | C | T | 14 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(11): Show |
14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2120-7694C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109245 | |||||||
chr1:175109249 | C | T | 10 | a0004c0008t0001g0173 a0004c0008t0001g0228 a0004c0008t0001g0329 others(7): Show |
10 | HG02015.hp2 NA18966.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.2120-7690C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109249 | |||||||
chr1:175109278 | C | T | 1 | a0007c0006t0001g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2120-7661C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109278 | |||||||
chr1:175109279 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2120-7660G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109279 | |||||||
chr1:175109310 | G | A | 1 | a0011c0011t0001g0240 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2120-7629G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109310 | |||||||
chr1:175109329 | G | C | 232 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2120-7610G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109329 | |||||||
chr1:175109339 | C | T | 94 | a0001c0016t0001g0355 a0002c0005t0004g0009 a0003c0002t0001g0266 others(91): Show |
95 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.2120-7600C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109339 | |||||||
chr1:175109377 | C | T | 3 | a0002c0029t0001g0055 a0002c0029t0003g0053 a0002c0029t0003g0054 |
3 | HG02630.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2120-7562C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109377 | |||||||
chr1:175109383 | C | T | 1 | a0003c0002t0001g0292 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2120-7556C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109383 | |||||||
chr1:175109384 | G | A | 2 | a0001c0001t0001g0062 a0001c0080t0008g0128 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2120-7555G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109384 | |||||||
chr1:175109542 | T | C | 5 | a0001c0073t0001g0052 a0002c0029t0001g0055 a0002c0029t0003g0053 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-7397T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109542 | |||||||
chr1:175109674 | T | A | 2 | a0002c0005t0007g0057 a0002c0077t0001g0095 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2120-7265T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109674 | |||||||
chr1:175109675 | A | T | 2 | a0002c0005t0007g0057 a0002c0077t0001g0095 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2120-7264A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109675 | |||||||
chr1:175109722 | A | G | 14 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2120-7217A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109722 | |||||||
chr1:175109891 | A | G | 87 | a0003c0002t0001g0266 a0003c0002t0001g0270 a0003c0002t0001g0278 others(84): Show |
88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2120-7048A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109891 | |||||||
chr1:175110015 | C | G | 11 | a0001c0016t0001g0040 a0002c0009t0001g0036 a0002c0009t0001g0037 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2120-6924C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110015 | |||||||
chr1:175110110 | T | C | 3 | a0019c0023t0001g0309 a0021c0056t0006g0274 a0021c0058t0006g0316 |
3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2120-6829T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110110 | |||||||
chr1:175110125 | C | T | 14 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2120-6814C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110125 | |||||||
chr1:175110234 | A | G | 3 | a0001c0016t0001g0040 a0002c0009t0001g0041 a0002c0009t0001g0042 |
3 | HG02257.hp2 HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2120-6705A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110234 | |||||||
chr1:175110498 | A | G | 56 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(53): Show |
56 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.2120-6441A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110498 | |||||||
chr1:175110528 | T | C | 1 | a0018c0020t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2120-6411T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110528 | |||||||
chr1:175110746 | T | G | 2 | a0041c0094t0001g0308 a0043c0093t0003g0307 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2120-6193T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110746 | |||||||
chr1:175110883 | T | G | 149 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2120-6056T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110883 | |||||||
chr1:175111050 | G | A | 8 | a0003c0002t0001g0266 a0003c0015t0001g0264 a0003c0015t0001g0312 others(5): Show |
8 | NA18955.hp2 NA18969.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.2120-5889G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111050 | |||||||
chr1:175111066 | C | T | 5 | a0002c0005t0007g0057 a0002c0077t0001g0095 a0026c0034t0003g0167 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-5873C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111066 | |||||||
chr1:175111089 | A | G | 149 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2120-5850A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111089 | |||||||
chr1:175111120 | C | A | 1 | a0008c0007t0002g0129 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2120-5819C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111120 | |||||||
chr1:175111233 | G | A | 3 | a0004c0008t0001g0329 a0004c0008t0002g0327 a0004c0008t0002g0328 |
3 | NA19009.hp1 NA19056.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2120-5706G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111233 | |||||||
chr1:175111345 | GGCATGAT others(7): Show |
G | 5 | a0003c0002t0001g0297 a0003c0002t0001g0299 a0003c0002t0001g0321 others(2): Show |
5 | HG02040.hp1 HG02523.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-5591_2120-557 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111345 | ||||||
chr1:175111425 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2120-5514C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111425 | |||||||
chr1:175111426 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2120-5513G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111426 | |||||||
chr1:175111486 | C | CA | 7 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0002c0077t0001g0095 others(4): Show |
7 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2120-5423dupA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | ||||||
chr1:175111486 | CA | C | 105 | a0001c0016t0001g0356 a0001c0016t0001g0360 a0001c0016t0001g0362 others(102): Show |
106 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.2120-5423delA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | ||||||
chr1:175111486 | CAA | C | 41 | a0001c0001t0001g0165 a0001c0016t0001g0355 a0001c0087t0001g0024 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.2120-5424_2120-542 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | ||||||
chr1:175111486 | CAAA | C | 122 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(119): Show |
123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.2120-5425_2120-542 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | ||||||
chr1:175111486 | CAAAA | C | 35 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(32): Show |
35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.2120-5426_2120-542 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | ||||||
chr1:175111486 | CAAAAAAA others(10): Show |
C | 11 | a0001c0016t0001g0040 a0002c0009t0001g0036 a0002c0009t0001g0037 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2120-5439_2120-542 others(21): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | ||||||
chr1:175111649 | G | T | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-5290G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111649 | |||||||
chr1:175111703 | C | A | 1 | a0034c0089t0003g0103 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2120-5236C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111703 | |||||||
chr1:175111778 | A | AT | 23 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0123 others(20): Show |
23 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2120-5150dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111778 | ||||||
chr1:175111778 | AT | A | 62 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(59): Show |
62 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.2120-5150delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111778 | ||||||
chr1:175111823 | C | T | 1 | a0001c0016t0001g0362 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2120-5116C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111823 | |||||||
chr1:175111854 | A | G | 5 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-5085A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111854 | |||||||
chr1:175111863 | G | A | 11 | a0001c0042t0001g0082 a0001c0042t0001g0098 a0002c0005t0007g0057 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2120-5076G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111863 | |||||||
chr1:175112246 | TA | T | 14 | a0001c0001t0001g0343 a0001c0001t0001g0351 a0013c0014t0001g0056 others(11): Show |
14 | HG01358.hp1 HG01891.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.2120-4692delA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112246 | |||||||
chr1:175112304 | T | C | 1 | a0003c0002t0001g0313 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2120-4635T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112304 | |||||||
chr1:175112320 | A | G | 5 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-4619A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112320 | |||||||
chr1:175112485 | T | C | 2 | a0004c0008t0002g0224 a0004c0008t0002g0225 |
2 | NA18998.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2120-4454T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112485 | |||||||
chr1:175112531 | G | A | 12 | a0001c0016t0001g0040 a0002c0009t0001g0036 a0002c0009t0001g0037 others(9): Show |
12 | HG01081.hp1 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2120-4408G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112531 | |||||||
chr1:175112588 | G | A | 2 | a0015c0024t0001g0161 a0015c0024t0001g0162 |
2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2120-4351G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112588 | |||||||
chr1:175112595 | G | A | 5 | a0001c0016t0001g0360 a0001c0016t0001g0362 a0002c0009t0002g0358 others(2): Show |
5 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-4344G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112595 | |||||||
chr1:175112598 | C | CT | 30 | a0004c0008t0001g0228 a0004c0008t0002g0171 a0004c0008t0002g0224 others(27): Show |
30 | HG00280.hp2 HG00639.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2120-4304dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTT | 52 | a0003c0002t0001g0283 a0003c0002t0001g0325 a0003c0015t0001g0264 others(49): Show |
52 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.2120-4305_2120-430 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTT | 72 | a0001c0001t0001g0351 a0003c0002t0001g0266 a0003c0002t0001g0270 others(69): Show |
73 | HG00609.hp1 HG00609.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.2120-4306_2120-430 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTT | 37 | a0002c0005t0002g0347 a0002c0029t0001g0055 a0002c0029t0003g0053 others(34): Show |
37 | HG00099.hp2 HG00544.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.2120-4307_2120-430 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTT | 16 | a0001c0001t0001g0338 a0001c0016t0001g0360 a0002c0009t0002g0363 others(13): Show |
16 | HG01069.hp2 HG01168.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.2120-4308_2120-430 others(9): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTT | 21 | a0001c0001t0001g0107 a0001c0001t0002g0122 a0001c0031t0005g0156 others(18): Show |
21 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2120-4309_2120-430 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT | 20 | a0001c0001t0001g0093 a0001c0001t0001g0123 a0001c0001t0001g0160 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2120-4310_2120-430 others(11): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(1): Show |
9 | a0001c0001t0001g0141 a0001c0001t0001g0151 a0001c0001t0001g0331 others(6): Show |
9 | HG00280.hp1 HG01106.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.2120-4311_2120-430 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(2): Show |
8 | a0001c0016t0001g0356 a0002c0005t0003g0105 a0002c0005t0003g0106 others(5): Show |
8 | HG01167.hp1 HG01192.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.2120-4312_2120-430 others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0062 a0001c0016t0001g0362 a0001c0028t0001g0364 others(3): Show |
6 | HG01261.hp2 HG01515.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.2120-4313_2120-430 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0158 a0001c0001t0001g0323 a0001c0081t0001g0159 others(4): Show |
7 | HG00140.hp2 HG01192.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2120-4314_2120-430 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(5): Show |
10 | a0001c0001t0001g0031 a0001c0001t0001g0108 a0001c0001t0001g0324 others(7): Show |
10 | HG01074.hp2 HG01109.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2120-4315_2120-430 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0345 a0001c0016t0001g0355 a0015c0024t0001g0162 others(1): Show |
4 | HG02615.hp2 HG03490.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.2120-4316_2120-430 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0001g0018 a0002c0037t0003g0357 a0002c0037t0003g0366 |
3 | HG02559.hp2 HG02809.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.2120-4318_2120-430 others(19): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0033c0067t0006g0100 |
3 | HG01943.hp1 HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2120-4319_2120-430 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(13): Show |
1 | a0015c0024t0002g0021 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2120-4323_2120-430 others(24): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0001g0343 a0013c0014t0001g0088 |
2 | HG04204.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2120-4324_2120-430 others(25): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0333 a0013c0014t0001g0083 |
2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2120-4326_2120-430 others(27): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2120-4327_2120-430 others(28): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0332 a0021c0057t0001g0175 |
2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2120-4328_2120-430 others(29): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0352 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2120-4329_2120-430 others(30): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(20): Show |
1 | a0001c0036t0001g0341 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2120-4330_2120-430 others(31): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(21): Show |
1 | a0036c0076t0003g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2120-4331_2120-430 others(32): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(22): Show |
1 | a0001c0036t0001g0342 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2120-4332_2120-430 others(33): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(23): Show |
1 | a0001c0031t0005g0330 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2120-4333_2120-430 others(34): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(24): Show |
1 | a0013c0014t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2120-4334_2120-430 others(35): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(27): Show |
1 | a0013c0014t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2120-4337_2120-430 others(38): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | C | CTTTTTTT others(29): Show |
1 | a0013c0014t0001g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2120-4339_2120-430 others(40): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | CTTT | C | 7 | a0002c0009t0001g0036 a0002c0009t0001g0037 a0002c0009t0001g0038 others(4): Show |
7 | HG02055.hp2 HG02922.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2120-4306_2120-430 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | CTTTTTTT others(3): Show |
C | 7 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(4): Show |
7 | HG02109.hp2 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2120-4313_2120-430 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0001g0334 a0001c0042t0001g0082 a0002c0026t0001g0002 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2120-4314_2120-430 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | CTTTTTTT others(6): Show |
C | 1 | a0002c0009t0003g0361 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2120-4316_2120-430 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0001g0165 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-4318_2120-430 others(19): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | CTTTTTTT others(9): Show |
C | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2120-4319_2120-430 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112598 | CTTTTTTT others(10): Show |
C | 1 | a0003c0047t0001g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2120-4320_2120-430 others(21): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | ||||||
chr1:175112771 | C | T | 3 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 |
3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2120-4168C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112771 | |||||||
chr1:175112784 | AT | A | 11 | a0001c0016t0001g0040 a0002c0009t0001g0036 a0002c0009t0001g0037 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2120-4146delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112784 | ||||||
chr1:175112917 | C | T | 6 | a0001c0042t0001g0082 a0001c0042t0001g0098 a0002c0026t0001g0002 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2120-4022C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112917 | |||||||
chr1:175112926 | C | T | 14 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0016t0001g0360 others(11): Show |
14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2120-4013C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112926 | |||||||
chr1:175112978 | T | C | 1 | a0041c0094t0001g0308 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2120-3961T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112978 | |||||||
chr1:175113168 | C | T | 87 | a0003c0002t0001g0266 a0003c0002t0001g0270 a0003c0002t0001g0278 others(84): Show |
88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2120-3771C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113168 | |||||||
chr1:175113245 | G | A | 1 | a0003c0047t0001g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2120-3694G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113245 | |||||||
chr1:175113332 | C | T | 1 | a0002c0005t0002g0347 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2120-3607C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113332 | |||||||
chr1:175113367 | C | G | 1 | a0006c0004t0002g0242 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2120-3572C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113367 | |||||||
chr1:175113427 | T | C | 6 | a0001c0073t0001g0052 a0002c0029t0001g0055 a0002c0029t0003g0053 others(3): Show |
6 | HG01069.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2120-3512T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113427 | |||||||
chr1:175113614 | G | A | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2120-3325G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113614 | |||||||
chr1:175113805 | C | A | 1 | a0002c0009t0003g0359 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2120-3134C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113805 | |||||||
chr1:175113832 | G | C | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2120-3107G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113832 | |||||||
chr1:175113840 | C | A | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-3099C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113840 | |||||||
chr1:175113909 | G | A | 1 | a0058c0062t0001g0196 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2120-3030G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113909 | |||||||
chr1:175113921 | T | C | 5 | a0003c0002t0001g0283 a0003c0002t0001g0317 a0003c0002t0012g0277 others(2): Show |
5 | HG02698.hp1 HG02735.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-3018T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113921 | |||||||
chr1:175114156 | T | G | 60 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2120-2783T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114156 | |||||||
chr1:175114275 | G | A | 51 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(48): Show |
51 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.2120-2664G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114275 | |||||||
chr1:175114584 | T | C | 1 | a0002c0009t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2120-2355T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114584 | |||||||
chr1:175114736 | GGAA | G | 56 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(53): Show |
56 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.2120-2195_2120-219 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175114736 | ||||||
chr1:175114770 | T | G | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-2169T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114770 | |||||||
chr1:175114816 | T | C | 60 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2120-2123T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114816 | |||||||
chr1:175114874 | A | G | 280 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(277): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.2120-2065A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114874 | |||||||
chr1:175114886 | G | A | 1 | a0003c0047t0001g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2120-2053G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114886 | |||||||
chr1:175115247 | A | G | 5 | a0008c0007t0001g0075 a0008c0007t0002g0072 a0008c0007t0002g0139 others(2): Show |
5 | NA18962.hp1 NA18971.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-1692A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115247 | |||||||
chr1:175115282 | C | T | 1 | a0031c0068t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2120-1657C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115282 | |||||||
chr1:175115332 | AGG | A | 46 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(43): Show |
46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2120-1606_2120-160 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115332 | |||||||
chr1:175115336 | G | A | 46 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(43): Show |
46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2120-1603G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115336 | |||||||
chr1:175115339 | GA | G | 46 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(43): Show |
46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2120-1597delA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175115339 | ||||||
chr1:175115341 | A | C | 46 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(43): Show |
46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2120-1598A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115341 | |||||||
chr1:175115344 | TAGTGC | T | 46 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(43): Show |
46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2120-1591_2120-158 others(9): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175115344 | ||||||
chr1:175115494 | C | T | 6 | a0001c0042t0001g0082 a0001c0042t0001g0098 a0002c0026t0001g0002 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2120-1445C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115494 | |||||||
chr1:175115613 | G | A | 2 | a0002c0005t0007g0057 a0002c0077t0001g0095 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2120-1326G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115613 | |||||||
chr1:175115681 | C | T | 2 | a0027c0039t0009g0010 a0027c0039t0009g0012 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2120-1258C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115681 | |||||||
chr1:175115688 | G | A | 6 | a0001c0073t0001g0052 a0002c0029t0001g0055 a0002c0029t0003g0053 others(3): Show |
6 | HG01069.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2120-1251G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115688 | |||||||
chr1:175115699 | A | G | 4 | a0001c0042t0001g0082 a0002c0026t0001g0002 a0002c0026t0003g0085 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-1240A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115699 | |||||||
chr1:175115721 | C | G | 54 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(51): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2120-1218C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115721 | |||||||
chr1:175115769 | C | T | 1 | a0016c0018t0001g0275 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2120-1170C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115769 | |||||||
chr1:175116046 | A | AT | 6 | a0002c0005t0007g0057 a0002c0077t0001g0095 a0007c0072t0001g0051 others(3): Show |
6 | HG02109.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2120-883dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175116046 | ||||||
chr1:175116084 | T | C | 1 | a0001c0001t0001g0331 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2120-855T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175116084 | |||||||
chr1:175116178 | A | G | 3 | a0002c0005t0001g0114 a0002c0005t0003g0149 a0002c0005t0003g0150 |
3 | HG00140.hp1 HG02257.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2120-761A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175116178 | |||||||
chr1:175116218 | C | CT | 5 | a0002c0005t0007g0057 a0002c0077t0001g0095 a0026c0034t0003g0167 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-713dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175116218 | ||||||
chr1:175116235 | G | A | 12 | a0001c0016t0001g0040 a0002c0009t0001g0036 a0002c0009t0001g0037 others(9): Show |
12 | HG01081.hp1 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2120-704G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175116235 | |||||||
chr1:175116439 | G | GAAGTA | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-496_2120-492d others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175116439 | ||||||
chr1:175116687 | C | T | 1 | a0004c0019t0001g0209 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2120-252C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175116687 | |||||||
chr1:175116693 | T | C | 2 | a0001c0042t0001g0098 a0045c0088t0005g0102 |
2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2120-246T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175116693 | |||||||
chr1:175117325 | A | G | 236 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2386+120A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175117325 | |||||||
chr1:175117816 | G | A | 1 | a0004c0019t0001g0353 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2386+611G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175117816 | |||||||
chr1:175117829 | T | G | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2386+624T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175117829 | |||||||
chr1:175117845 | C | T | 1 | a0002c0005t0002g0019 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2386+640C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175117845 | |||||||
chr1:175117900 | T | G | 1 | a0005c0003t0001g0255 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2387-661T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175117900 | |||||||
chr1:175118111 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2387-450C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175118111 | |||||||
chr1:175118213 | C | A | 1 | a0030c0045t0001g0207 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2387-348C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175118213 | |||||||
chr1:175118470 | T | C | 56 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(53): Show |
56 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.2387-91T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175118470 | |||||||
chr1:175118484 | C | T | 3 | a0039c0070t0004g0015 a0042c0071t0004g0013 a0044c0069t0004g0014 |
3 | HG02622.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2387-77C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175118484 | |||||||
chr1:175118541 | G | A | 154 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(151): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.2387-20G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175118541 | |||||||
chr1:175118547 | A | AT | 61 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(58): Show |
61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
splice_region_variant&intron_variant | LOW | c.2387-4dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 175118547 | ||||||
chr1:175118933 | A | G | 1 | a0008c0007t0002g0134 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2650+109A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175118933 | |||||||
chr1:175118992 | G | A | 1 | a0001c0016t0001g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2650+168G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175118992 | |||||||
chr1:175119030 | G | A | 1 | a0009c0021t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2650+206G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119030 | |||||||
chr1:175119051 | G | A | 60 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2650+227G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119051 | |||||||
chr1:175119172 | C | T | 2 | a0004c0008t0002g0224 a0004c0008t0002g0225 |
2 | NA18998.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2650+348C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119172 | |||||||
chr1:175119309 | A | G | 2 | a0013c0014t0001g0083 a0013c0014t0001g0088 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2650+485A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119309 | |||||||
chr1:175119401 | C | T | 60 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0107 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2650+577C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119401 | |||||||
chr1:175119516 | A | G | 89 | a0004c0008t0001g0173 a0004c0008t0001g0228 a0004c0008t0001g0329 others(86): Show |
89 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2650+692A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119516 | |||||||
chr1:175119629 | C | CTT | 26 | a0001c0001t0001g0331 a0001c0016t0001g0356 a0001c0016t0001g0360 others(23): Show |
27 | HG01070.hp2 HG01071.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2650+812_2650+813d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175119629 | ||||||
chr1:175119629 | C | CTTT | 69 | a0001c0016t0001g0355 a0001c0073t0001g0052 a0002c0009t0002g0363 others(66): Show |
70 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.2650+811_2650+813d others(5): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175119629 | ||||||
chr1:175119629 | C | CTTTT | 27 | a0002c0029t0003g0054 a0003c0002t0001g0266 a0003c0002t0001g0291 others(24): Show |
27 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.2650+810_2650+813d others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175119629 | ||||||
chr1:175119637 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2650+813T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119637 | |||||||
chr1:175119637 | TC | T | 4 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2650+814delC | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119637 | |||||||
chr1:175119638 | C | CT | 14 | a0001c0016t0001g0040 a0002c0009t0001g0036 a0002c0009t0001g0037 others(11): Show |
14 | HG00738.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2650+830dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175119638 | ||||||
chr1:175119638 | C | T | 133 | a0001c0001t0001g0125 a0001c0001t0001g0165 a0001c0001t0001g0331 others(130): Show |
135 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.2650+814C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119638 | |||||||
chr1:175119650 | T | C | 1 | a0008c0007t0002g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2650+826T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119650 | |||||||
chr1:175119658 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2650+834A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119658 | |||||||
chr1:175119720 | C | T | 85 | a0003c0002t0001g0266 a0003c0002t0001g0270 a0003c0002t0001g0278 others(82): Show |
86 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.2650+896C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119720 | |||||||
chr1:175119727 | C | T | 2 | a0001c0073t0001g0052 a0007c0072t0001g0051 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2650+903C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119727 | |||||||
chr1:175119779 | C | T | 1 | a0010c0010t0001g0113 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2650+955C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119779 | |||||||
chr1:175119783 | C | T | 1 | a0031c0068t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2650+959C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119783 | |||||||
chr1:175119791 | T | C | 1 | a0007c0006t0001g0349 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2650+967T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119791 | |||||||
chr1:175119795 | C | T | 2 | a0010c0010t0001g0111 a0010c0010t0001g0113 |
2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2650+971C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119795 | |||||||
chr1:175119816 | T | A | 2 | a0001c0073t0001g0052 a0007c0072t0001g0051 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2650+992T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119816 | |||||||
chr1:175119912 | A | G | 98 | a0001c0016t0001g0355 a0001c0016t0001g0356 a0001c0028t0001g0364 others(95): Show |
99 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.2650+1088A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119912 | |||||||
chr1:175119929 | C | T | 2 | a0001c0001t0001g0093 a0001c0042t0001g0082 |
2 | HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2650+1105C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119929 | |||||||
chr1:175119946 | G | A | 49 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(46): Show |
49 | HG00099.hp2 HG01106.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.2650+1122G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119946 | |||||||
chr1:175119958 | T | C | 43 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(40): Show |
43 | HG00099.hp2 HG01106.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.2650+1134T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119958 | |||||||
chr1:175119993 | C | T | 5 | a0002c0005t0004g0009 a0007c0006t0004g0008 a0007c0006t0015g0011 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+1169C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119993 | |||||||
chr1:175120121 | T | C | 8 | a0001c0001t0001g0158 a0001c0042t0001g0098 a0002c0026t0003g0085 others(5): Show |
8 | HG02622.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2650+1297T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120121 | |||||||
chr1:175120288 | C | T | 2 | a0041c0094t0001g0308 a0043c0093t0003g0307 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2650+1464C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120288 | |||||||
chr1:175120307 | T | C | 3 | a0001c0001t0001g0141 a0001c0016t0001g0356 a0002c0005t0001g0142 |
3 | HG03516.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2650+1483T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120307 | |||||||
chr1:175120407 | C | T | 1 | a0007c0038t0011g0368 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2650+1583C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120407 | |||||||
chr1:175120411 | C | G | 1 | a0004c0019t0001g0353 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2650+1587C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120411 | |||||||
chr1:175120436 | T | C | 11 | a0001c0016t0008g0045 a0001c0028t0007g0044 a0001c0028t0007g0046 others(8): Show |
11 | HG01069.hp1 HG01192.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2650+1612T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120436 | |||||||
chr1:175120475 | C | T | 13 | a0001c0001t0001g0093 a0001c0001t0001g0323 a0001c0001t0001g0350 others(10): Show |
13 | HG01192.hp1 HG01433.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.2650+1651C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120475 | |||||||
chr1:175120520 | G | A | 7 | a0002c0005t0001g0142 a0027c0039t0009g0010 a0027c0039t0009g0012 others(4): Show |
7 | HG02451.hp1 HG02723.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2650+1696G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120520 | |||||||
chr1:175120529 | T | C | 2 | a0004c0008t0002g0206 a0007c0006t0001g0094 |
2 | HG02523.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2650+1705T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120529 | |||||||
chr1:175120632 | T | C | 4 | a0003c0002t0001g0305 a0006c0004t0001g0191 a0006c0004t0001g0213 others(1): Show |
4 | HG00738.hp2 HG01123.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2650+1808T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120632 | |||||||
chr1:175120665 | C | T | 1 | a0054c0083t0001g0076 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2650+1841C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120665 | |||||||
chr1:175120738 | TG | T | 49 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0031 others(46): Show |
50 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.2650+1916delG | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175120738 | ||||||
chr1:175120827 | G | T | 88 | a0002c0005t0002g0019 a0003c0002t0001g0266 a0003c0002t0001g0270 others(85): Show |
88 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.2650+2003G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120827 | |||||||
chr1:175120958 | A | G | 202 | a0001c0016t0001g0360 a0001c0016t0001g0362 a0001c0031t0005g0063 others(199): Show |
203 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.2650+2134A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120958 | |||||||
chr1:175121035 | G | A | 1 | a0053c0092t0001g0227 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2650+2211G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121035 | |||||||
chr1:175121278 | A | G | 313 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(310): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2651-2122A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121278 | |||||||
chr1:175121290 | T | C | 2 | a0021c0056t0006g0274 a0021c0058t0006g0316 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2651-2110T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121290 | |||||||
chr1:175121301 | C | G | 310 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(307): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2651-2099C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121301 | |||||||
chr1:175121312 | G | A | 4 | a0007c0006t0001g0337 a0007c0006t0001g0370 a0041c0094t0001g0308 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2651-2088G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121312 | |||||||
chr1:175121418 | C | T | 216 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.2651-1982C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121418 | |||||||
chr1:175121499 | T | G | 2 | a0007c0006t0001g0369 a0007c0006t0015g0011 |
2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2651-1901T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121499 | |||||||
chr1:175121592 | G | A | 1 | a0003c0002t0001g0291 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2651-1808G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121592 | |||||||
chr1:175121631 | C | A | 212 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.2651-1769C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121631 | |||||||
chr1:175121701 | GGAT | G | 213 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2651-1695_2651-169 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175121701 | ||||||
chr1:175121803 | T | C | 2 | a0041c0094t0001g0308 a0043c0093t0003g0307 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2651-1597T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121803 | |||||||
chr1:175121822 | G | C | 116 | a0001c0036t0001g0342 a0003c0002t0001g0266 a0003c0002t0001g0270 others(113): Show |
116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.2651-1578G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121822 | |||||||
chr1:175121844 | G | A | 213 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2651-1556G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121844 | |||||||
chr1:175121958 | A | C | 1 | a0002c0005t0001g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2651-1442A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121958 | |||||||
chr1:175122015 | G | A | 85 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(82): Show |
86 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2651-1385G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122015 | |||||||
chr1:175122201 | G | T | 1 | a0049c0084t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2651-1199G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122201 | |||||||
chr1:175122218 | C | CAA | 213 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2651-1171_2651-117 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175122218 | ||||||
chr1:175122218 | C | CAAA | 9 | a0001c0001t0001g0331 a0001c0001t0001g0334 a0001c0031t0005g0063 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651-1172_2651-117 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175122218 | ||||||
chr1:175122417 | C | T | 4 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(1): Show |
4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2651-983C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122417 | |||||||
chr1:175122455 | TTGCTAAC others(45): Show |
T | 213 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2651-942_2651-891d others(54): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175122455 | ||||||
chr1:175122510 | T | A | 213 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2651-890T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122510 | |||||||
chr1:175122518 | G | A | 9 | a0001c0001t0001g0331 a0001c0028t0001g0364 a0001c0028t0007g0044 others(6): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651-882G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122518 | |||||||
chr1:175122579 | C | G | 4 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0333 others(1): Show |
4 | HG02896.hp2 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2651-821C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122579 | |||||||
chr1:175122847 | T | A | 85 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(82): Show |
86 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2651-553T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122847 | |||||||
chr1:175122847 | T | C | 9 | a0001c0001t0001g0331 a0001c0028t0001g0364 a0001c0028t0007g0044 others(6): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651-553T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122847 | |||||||
chr1:175122909 | A | C | 2 | a0038c0085t0001g0335 a0057c0078t0001g0164 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2651-491A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122909 | |||||||
chr1:175122997 | C | A | 84 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(81): Show |
85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.2651-403C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122997 | |||||||
chr1:175123000 | C | G | 120 | a0003c0002t0001g0266 a0003c0002t0001g0270 a0003c0002t0001g0278 others(117): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2651-400C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175123000 | |||||||
chr1:175123014 | G | A | 9 | a0001c0001t0001g0331 a0001c0028t0001g0364 a0001c0028t0007g0044 others(6): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651-386G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175123014 | |||||||
chr1:175123226 | T | C | 1 | a0002c0005t0003g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2651-174T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175123226 | |||||||
chr1:175123686 | G | A | 1 | a0012c0013t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2914+23G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123686 | |||||||
chr1:175123704 | T | C | 214 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2914+41T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123704 | |||||||
chr1:175123767 | C | T | 3 | a0002c0009t0003g0365 a0002c0037t0003g0357 a0002c0037t0003g0366 |
3 | HG02559.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2914+104C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123767 | |||||||
chr1:175123781 | A | G | 1 | a0001c0031t0005g0330 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2914+118A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123781 | |||||||
chr1:175123856 | GGAGT | G | 288 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.2914+199_2914+202d others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175123856 | ||||||
chr1:175123887 | C | T | 1 | a0020c0022t0001g0298 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2914+224C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123887 | |||||||
chr1:175123954 | A | G | 2 | a0008c0007t0002g0059 a0008c0007t0002g0060 |
2 | NA18948.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2914+291A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123954 | |||||||
chr1:175124235 | G | T | 213 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2914+572G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124235 | |||||||
chr1:175124407 | G | A | 4 | a0027c0039t0009g0010 a0027c0039t0009g0012 a0028c0043t0001g0032 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2914+744G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124407 | |||||||
chr1:175124408 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2914+745C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124408 | |||||||
chr1:175124447 | A | G | 226 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.2914+784A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124447 | |||||||
chr1:175124632 | G | T | 119 | a0003c0002t0001g0266 a0003c0002t0001g0270 a0003c0002t0001g0278 others(116): Show |
119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2914+969G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124632 | |||||||
chr1:175124687 | GCAAA | G | 74 | a0002c0005t0004g0009 a0002c0005t0007g0057 a0002c0009t0001g0036 others(71): Show |
75 | HG00639.hp1 HG01070.hp1 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.2914+1050_2914+105 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175124687 | ||||||
chr1:175124687 | GCAAACAA others(1): Show |
G | 213 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2914+1046_2914+105 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175124687 | ||||||
chr1:175124731 | T | C | 310 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(307): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2914+1068T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124731 | |||||||
chr1:175124889 | G | A | 85 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(82): Show |
86 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2914+1226G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124889 | |||||||
chr1:175125363 | T | TA | 62 | a0002c0005t0007g0057 a0002c0026t0003g0085 a0002c0026t0003g0086 others(59): Show |
62 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.2915-1581dupA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125363 | ||||||
chr1:175125461 | TC | T | 3 | a0002c0026t0003g0085 a0002c0026t0003g0086 a0033c0067t0006g0100 |
3 | HG01943.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2915-1491delC | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125461 | ||||||
chr1:175125516 | ATCCCTTC others(4): Show |
A | 2 | a0005c0003t0001g0169 a0005c0003t0001g0181 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2915-1433_2915-142 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125516 | ||||||
chr1:175125517 | T | A | 1 | a0005c0003t0001g0258 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2915-1438T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125517 | |||||||
chr1:175125586 | CCTCTTTC others(3): Show |
C | 1 | a0001c0001t0001g0350 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2915-1356_2915-134 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125586 | ||||||
chr1:175125666 | TCTCC | T | 61 | a0002c0005t0007g0057 a0002c0026t0003g0085 a0002c0026t0003g0086 others(58): Show |
61 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.2915-1276_2915-127 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125666 | ||||||
chr1:175125670 | C | T | 1 | a0004c0019t0002g0237 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2915-1285C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125670 | |||||||
chr1:175125684 | T | C | 214 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2915-1271T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125684 | |||||||
chr1:175125685 | T | C | 1 | a0008c0007t0002g0134 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2915-1270T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125685 | |||||||
chr1:175125697 | TTTTCTCT others(5): Show |
T | 1 | a0008c0007t0002g0136 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2915-1252_2915-124 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125697 | ||||||
chr1:175125699 | TTC | T | 43 | a0001c0001t0001g0023 a0001c0001t0001g0323 a0001c0001t0001g0333 others(40): Show |
43 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2915-1250_2915-124 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125699 | ||||||
chr1:175125701 | CTCTCTT | C | 39 | a0001c0001t0001g0031 a0001c0001t0001g0107 a0001c0001t0001g0108 others(36): Show |
39 | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.2915-1250_2915-124 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | ||||||
chr1:175125701 | CTCTCTTT others(3): Show |
C | 68 | a0001c0001t0001g0020 a0001c0001t0001g0062 a0001c0001t0001g0093 others(65): Show |
69 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2915-1250_2915-124 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | ||||||
chr1:175125701 | CTCTCTTT others(7): Show |
C | 18 | a0001c0001t0001g0160 a0001c0001t0001g0350 a0001c0016t0001g0040 others(15): Show |
18 | HG00408.hp2 HG00738.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2915-1250_2915-123 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | ||||||
chr1:175125701 | CTCTCTTT others(11): Show |
C | 11 | a0001c0001t0001g0165 a0001c0001t0001g0352 a0001c0016t0001g0356 others(8): Show |
11 | HG00642.hp2 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2915-1250_2915-123 others(22): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | ||||||
chr1:175125701 | CTCTCTTT others(15): Show |
C | 5 | a0013c0014t0001g0056 a0027c0039t0009g0010 a0027c0039t0009g0012 others(2): Show |
5 | HG01358.hp1 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2915-1250_2915-122 others(26): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | ||||||
chr1:175125701 | CTCTCTTT others(27): Show |
C | 1 | a0006c0061t0002g0217 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2915-1250_2915-121 others(38): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | ||||||
chr1:175125703 | C | CTCTTTCT others(5): Show |
1 | a0008c0040t0003g0146 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2915-1208_2915-119 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125703 | C | CTT | 22 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0158 others(19): Show |
22 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.2915-1251_2915-125 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125703 | C | CTTTCTT | 5 | a0001c0001t0001g0344 a0001c0016t0001g0360 a0003c0015t0001g0312 others(2): Show |
5 | HG01255.hp1 HG01517.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2915-1251_2915-125 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125703 | C | CTTTCTTT others(3): Show |
1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2915-1251_2915-125 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125703 | CTCTT | C | 26 | a0002c0005t0016g0030 a0004c0008t0002g0199 a0004c0008t0002g0226 others(23): Show |
27 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.2915-1200_2915-119 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125703 | CTCTTTCT others(1): Show |
C | 38 | a0002c0005t0002g0117 a0002c0005t0002g0346 a0002c0005t0004g0009 others(35): Show |
38 | HG00642.hp1 HG01081.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.2915-1204_2915-119 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125703 | CTCTTTCT others(5): Show |
C | 23 | a0002c0005t0001g0114 a0002c0005t0001g0121 a0002c0005t0002g0019 others(20): Show |
24 | HG00140.hp1 HG00323.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.2915-1208_2915-119 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125703 | CTCTTTCT others(9): Show |
C | 20 | a0002c0005t0002g0022 a0002c0005t0007g0057 a0002c0009t0001g0038 others(17): Show |
20 | HG01243.hp1 HG01256.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.2915-1212_2915-119 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125703 | CTCTTTCT others(13): Show |
C | 5 | a0002c0009t0001g0049 a0004c0054t0002g0193 a0017c0025t0001g0081 others(2): Show |
5 | HG02129.hp2 NA18906.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.2915-1216_2915-119 others(24): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125703 | CTCTTTCT others(25): Show |
C | 22 | a0002c0005t0001g0142 a0002c0005t0003g0104 a0002c0005t0003g0105 others(19): Show |
22 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.2915-1228_2915-119 others(36): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125703 | CTCTTTCT others(37): Show |
C | 1 | a0039c0070t0004g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2915-1240_2915-119 others(48): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | ||||||
chr1:175125745 | CTTTCTTT others(3): Show |
C | 1 | a0011c0011t0001g0240 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2915-1208_2915-119 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125745 | ||||||
chr1:175125753 | CTT | C | 4 | a0007c0006t0001g0337 a0007c0006t0001g0370 a0041c0094t0001g0308 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2915-1200_2915-119 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125753 | ||||||
chr1:175125755 | T | C | 1 | a0007c0006t0001g0369 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2915-1200T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125755 | |||||||
chr1:175125759 | C | T | 1 | a0012c0013t0001g0061 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2915-1196C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125759 | |||||||
chr1:175125811 | C | T | 288 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.2915-1144C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125811 | |||||||
chr1:175125818 | CCTCCTTT others(18): Show |
C | 1 | a0029c0082t0001g0067 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2915-1136_2915-111 others(29): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125818 | |||||||
chr1:175125822 | CTTTCTTT others(14): Show |
C | 300 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.2915-1095_2915-107 others(25): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125822 | ||||||
chr1:175125823 | T | C | 13 | a0002c0005t0004g0009 a0002c0009t0001g0036 a0002c0009t0001g0037 others(10): Show |
14 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2915-1132T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125823 | |||||||
chr1:175125825 | T | C | 13 | a0002c0005t0004g0009 a0002c0009t0001g0036 a0002c0009t0001g0037 others(10): Show |
14 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2915-1130T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125825 | |||||||
chr1:175125826 | CTTTCTTT others(10): Show |
C | 13 | a0002c0005t0004g0009 a0002c0009t0001g0036 a0002c0009t0001g0037 others(10): Show |
14 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2915-1117_2915-110 others(21): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125826 | ||||||
chr1:175125844 | T | C | 62 | a0002c0005t0007g0057 a0002c0026t0003g0085 a0002c0026t0003g0086 others(59): Show |
62 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.2915-1111T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125844 | |||||||
chr1:175125846 | T | C | 62 | a0002c0005t0007g0057 a0002c0026t0003g0085 a0002c0026t0003g0086 others(59): Show |
62 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.2915-1109T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125846 | |||||||
chr1:175125893 | C | A | 1 | a0045c0088t0005g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2915-1062C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125893 | |||||||
chr1:175125963 | T | TTC | 173 | a0002c0005t0007g0057 a0002c0026t0003g0085 a0002c0026t0003g0086 others(170): Show |
173 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.2915-973_2915-972d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125963 | ||||||
chr1:175125963 | TTCTC | T | 3 | a0001c0001t0001g0334 a0001c0042t0001g0082 a0019c0023t0001g0241 |
3 | HG02486.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2915-975_2915-972d others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125963 | ||||||
chr1:175126057 | A | C | 1 | a0002c0005t0002g0019 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2915-898A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126057 | |||||||
chr1:175126077 | G | A | 1 | a0003c0002t0001g0266 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2915-878G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126077 | |||||||
chr1:175126104 | C | CT | 163 | a0002c0005t0007g0057 a0002c0026t0003g0085 a0002c0026t0003g0086 others(160): Show |
163 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2915-836dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175126104 | ||||||
chr1:175126104 | C | CTT | 15 | a0001c0001t0001g0333 a0001c0001t0001g0344 a0001c0016t0001g0360 others(12): Show |
15 | HG01255.hp1 HG01517.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2915-837_2915-836d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175126104 | ||||||
chr1:175126104 | C | CTTT | 100 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(97): Show |
102 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.2915-838_2915-836d others(5): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175126104 | ||||||
chr1:175126104 | C | CTTTT | 6 | a0001c0031t0005g0063 a0007c0006t0001g0337 a0007c0006t0001g0370 others(3): Show |
6 | HG02280.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2915-839_2915-836d others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175126104 | ||||||
chr1:175126161 | A | G | 124 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(121): Show |
126 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2915-794A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126161 | |||||||
chr1:175126258 | T | C | 286 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(283): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.2915-697T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126258 | |||||||
chr1:175126327 | C | A | 120 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(117): Show |
122 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2915-628C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126327 | |||||||
chr1:175126347 | G | A | 3 | a0001c0031t0005g0063 a0001c0031t0005g0156 a0001c0031t0005g0330 |
3 | HG01884.hp1 HG03471.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2915-608G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126347 | |||||||
chr1:175126397 | G | A | 1 | a0001c0042t0001g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2915-558G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126397 | |||||||
chr1:175126438 | G | A | 24 | a0002c0005t0001g0142 a0002c0005t0003g0104 a0002c0005t0003g0105 others(21): Show |
24 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.2915-517G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126438 | |||||||
chr1:175126440 | C | T | 119 | a0002c0005t0002g0019 a0002c0005t0002g0022 a0003c0002t0001g0266 others(116): Show |
119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2915-515C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126440 | |||||||
chr1:175126513 | T | C | 1 | a0045c0088t0005g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2915-442T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126513 | |||||||
chr1:175126729 | G | A | 2 | a0028c0043t0001g0032 a0028c0043t0001g0033 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2915-226G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126729 | |||||||
chr1:175126800 | C | T | 94 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(91): Show |
95 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.2915-155C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126800 | |||||||
chr1:175126884 | C | T | 3 | a0007c0006t0001g0084 a0021c0057t0001g0175 a0042c0071t0004g0013 |
3 | HG01069.hp1 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2915-71C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126884 | |||||||
chr1:175126885 | T | C | 3 | a0001c0001t0001g0334 a0001c0042t0001g0082 a0019c0023t0001g0241 |
3 | HG02486.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2915-70T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126885 | |||||||
chr1:175126918 | T | A | 2 | a0038c0085t0001g0335 a0057c0078t0001g0164 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2915-37T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126918 | |||||||
chr1:175127089 | C | T | 1 | a0011c0011t0001g0238 | 1 | HG00408.hp1 | splice_region_variant&intron_variant | LOW | c.3045+4C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127089 | |||||||
chr1:175127128 | G | A | 1 | a0013c0014t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3045+43G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127128 | |||||||
chr1:175127176 | G | T | 2 | a0007c0006t0001g0369 a0007c0006t0015g0011 |
2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3045+91G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127176 | |||||||
chr1:175127197 | A | G | 177 | a0001c0001t0001g0331 a0001c0016t0008g0045 a0001c0031t0005g0063 others(174): Show |
177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.3045+112A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127197 | |||||||
chr1:175127197 | A | T | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3045+112A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127197 | |||||||
chr1:175127242 | G | T | 1 | a0004c0032t0002g0192 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3045+157G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127242 | |||||||
chr1:175127253 | C | T | 176 | a0001c0001t0001g0331 a0001c0016t0008g0045 a0001c0031t0005g0063 others(173): Show |
176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.3045+168C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127253 | |||||||
chr1:175127254 | C | T | 3 | a0001c0016t0001g0356 a0014c0090t0001g0124 a0029c0082t0001g0067 |
3 | HG00642.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3045+169C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127254 | |||||||
chr1:175127437 | A | G | 1 | a0003c0002t0001g0313 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3045+352A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127437 | |||||||
chr1:175127589 | G | A | 98 | a0001c0001t0001g0331 a0002c0005t0007g0057 a0002c0009t0001g0049 others(95): Show |
98 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.3046-443G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127589 | |||||||
chr1:175127680 | G | A | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3046-352G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127680 | |||||||
chr1:175127774 | G | A | 64 | a0003c0015t0001g0264 a0003c0015t0001g0312 a0003c0015t0003g0261 others(61): Show |
64 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.3046-258G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127774 | |||||||
chr1:175127879 | C | T | 2 | a0001c0001t0001g0062 a0001c0080t0008g0128 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3046-153C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127879 | |||||||
chr1:175127958 | C | T | 27 | a0002c0005t0001g0142 a0002c0005t0003g0104 a0002c0005t0003g0105 others(24): Show |
27 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.3046-74C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127958 | |||||||
chr1:175128023 | G | A | 3 | a0007c0006t0001g0337 a0007c0006t0001g0370 a0041c0094t0001g0308 |
3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3046-9G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175128023 | |||||||
chr1:175128195 | G | A | 140 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(137): Show |
141 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.3178+31G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128195 | |||||||
chr1:175128213 | C | T | 235 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3178+49C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128213 | |||||||
chr1:175128221 | C | G | 102 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(99): Show |
102 | HG00639.hp1 HG01070.hp1 HG01109.hp2 others(99): Show |
intron_variant | MODIFIER | c.3178+57C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128221 | |||||||
chr1:175128263 | A | T | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3178+99A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128263 | |||||||
chr1:175128277 | G | A | 3 | a0002c0026t0003g0085 a0002c0026t0003g0086 a0033c0067t0006g0100 |
3 | HG01943.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3178+113G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128277 | |||||||
chr1:175128361 | G | C | 2 | a0021c0056t0006g0274 a0021c0058t0006g0316 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3178+197G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128361 | |||||||
chr1:175128411 | C | A | 2 | a0002c0005t0001g0121 a0008c0007t0002g0099 |
2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.3179-184C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128411 | |||||||
chr1:175128533 | G | A | 3 | a0004c0008t0002g0226 a0004c0008t0002g0229 a0009c0012t0002g0319 |
3 | NA18993.hp2 NA18995.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3179-62G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128533 | |||||||
chr1:175128574 | C | G | 1 | a0009c0021t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3179-21C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128574 | |||||||
chr1:175128775 | T | A | 26 | a0002c0005t0001g0142 a0002c0005t0003g0104 a0002c0005t0003g0105 others(23): Show |
26 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.3330+29T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128775 | |||||||
chr1:175128808 | G | A | 11 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(8): Show |
11 | HG01192.hp2 HG02145.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.3330+62G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128808 | |||||||
chr1:175128854 | C | A | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3330+108C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128854 | |||||||
chr1:175128855 | C | T | 170 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(167): Show |
171 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.3330+109C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128855 | |||||||
chr1:175128856 | C | T | 1 | a0009c0021t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3330+110C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128856 | |||||||
chr1:175128900 | G | A | 6 | a0003c0002t0001g0300 a0003c0002t0001g0303 a0006c0004t0001g0253 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.3330+154G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128900 | |||||||
chr1:175128911 | T | G | 34 | a0002c0005t0001g0142 a0002c0005t0003g0104 a0002c0005t0003g0105 others(31): Show |
34 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.3330+165T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128911 | |||||||
chr1:175129023 | A | G | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3330+277A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129023 | |||||||
chr1:175129064 | G | A | 7 | a0002c0009t0001g0037 a0002c0009t0001g0038 a0002c0009t0001g0039 others(4): Show |
7 | HG02257.hp2 HG02630.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.3330+318G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129064 | |||||||
chr1:175129159 | A | G | 1 | a0004c0032t0002g0192 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3330+413A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129159 | |||||||
chr1:175129318 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3330+572C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129318 | |||||||
chr1:175129400 | C | T | 5 | a0001c0001t0001g0331 a0002c0005t0007g0057 a0002c0009t0001g0049 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.3330+654C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129400 | |||||||
chr1:175129609 | C | T | 3 | a0007c0006t0001g0337 a0007c0006t0001g0370 a0041c0094t0001g0308 |
3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3330+863C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129609 | |||||||
chr1:175130140 | A | G | 1 | a0001c0016t0001g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3330+1394A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130140 | |||||||
chr1:175130153 | G | A | 1 | a0036c0076t0003g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3330+1407G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130153 | |||||||
chr1:175130194 | G | A | 4 | a0027c0039t0009g0010 a0027c0039t0009g0012 a0028c0043t0001g0032 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3330+1448G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130194 | |||||||
chr1:175130234 | A | C | 1 | a0007c0006t0001g0349 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3330+1488A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130234 | |||||||
chr1:175130386 | C | T | 1 | a0002c0009t0003g0359 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3330+1640C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130386 | |||||||
chr1:175130438 | C | T | 161 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(158): Show |
162 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.3330+1692C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130438 | |||||||
chr1:175130564 | C | T | 15 | a0001c0001t0001g0108 a0001c0001t0001g0165 a0001c0001t0001g0323 others(12): Show |
15 | HG00639.hp2 HG01074.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.3330+1818C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130564 | |||||||
chr1:175130610 | CAGA | C | 93 | a0003c0002t0001g0266 a0003c0002t0001g0270 a0003c0002t0001g0278 others(90): Show |
93 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.3330+1867_3330+186 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175130610 | ||||||
chr1:175130636 | T | C | 199 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(196): Show |
200 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.3330+1890T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130636 | |||||||
chr1:175130777 | C | G | 25 | a0002c0005t0001g0142 a0002c0005t0003g0104 a0002c0005t0003g0105 others(22): Show |
25 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.3330+2031C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130777 | |||||||
chr1:175130780 | A | G | 1 | a0026c0034t0003g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3330+2034A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130780 | |||||||
chr1:175130918 | G | C | 2 | a0007c0006t0001g0369 a0007c0006t0015g0011 |
2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3330+2172G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130918 | |||||||
chr1:175131038 | GT | G | 8 | a0021c0056t0006g0274 a0021c0058t0006g0316 a0027c0039t0009g0010 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3330+2299delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131038 | ||||||
chr1:175131172 | T | C | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3330+2426T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175131172 | |||||||
chr1:175131440 | G | T | 2 | a0002c0029t0003g0053 a0002c0029t0003g0054 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3330+2694G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175131440 | |||||||
chr1:175131446 | C | T | 197 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(194): Show |
198 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.3330+2700C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175131446 | |||||||
chr1:175131587 | C | CCTGTGGG others(6): Show |
1 | a0004c0019t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3330+2843_3330+285 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131587 | ||||||
chr1:175131727 | C | G | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3330+2981C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175131727 | |||||||
chr1:175131917 | T | TAC | 28 | a0001c0001t0001g0345 a0001c0031t0005g0156 a0002c0005t0002g0019 others(25): Show |
28 | HG00099.hp2 HG00408.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.3330+3209_3330+321 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131917 | T | TACAC | 24 | a0001c0001t0001g0108 a0001c0001t0001g0352 a0001c0016t0001g0362 others(21): Show |
24 | HG00280.hp2 HG00323.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.3330+3207_3330+321 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131917 | T | TACACAC | 58 | a0001c0001t0001g0031 a0001c0001t0001g0107 a0001c0001t0001g0158 others(55): Show |
59 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.3330+3205_3330+321 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131917 | T | TACACACA others(1): Show |
44 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(41): Show |
44 | HG01070.hp1 HG01081.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.3330+3203_3330+321 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131917 | T | TACACACA others(3): Show |
49 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0332 others(46): Show |
49 | HG00639.hp1 HG01243.hp1 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.3330+3201_3330+321 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131917 | T | TACACACA others(5): Show |
14 | a0001c0073t0001g0052 a0002c0026t0003g0085 a0002c0026t0003g0086 others(11): Show |
14 | HG01515.hp1 HG01517.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.3330+3199_3330+321 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131917 | T | TACACACA others(7): Show |
11 | a0002c0005t0003g0104 a0002c0005t0003g0105 a0002c0005t0003g0106 others(8): Show |
11 | HG01192.hp1 HG01255.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.3330+3197_3330+321 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131917 | T | TACACACA others(9): Show |
2 | a0005c0003t0003g0256 a0043c0093t0003g0307 |
2 | HG01934.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3330+3195_3330+321 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131917 | T | TACACACA others(11): Show |
1 | a0016c0018t0001g0320 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3330+3193_3330+321 others(22): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131917 | TAC | T | 5 | a0002c0005t0002g0347 a0003c0002t0001g0315 a0009c0012t0003g0273 others(2): Show |
5 | HG01109.hp2 HG02135.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.3330+3209_3330+321 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131917 | TACACAC | T | 6 | a0007c0006t0001g0006 a0007c0006t0001g0007 a0007c0006t0004g0008 others(3): Show |
6 | HG02809.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3330+3205_3330+321 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | ||||||
chr1:175131957 | T | C | 2 | a0001c0031t0005g0156 a0001c0031t0005g0330 |
2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3330+3211T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175131957 | |||||||
chr1:175132039 | G | T | 5 | a0007c0006t0001g0006 a0007c0006t0001g0007 a0007c0006t0004g0008 others(2): Show |
5 | HG02809.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3330+3293G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132039 | |||||||
chr1:175132079 | C | T | 103 | a0001c0001t0001g0331 a0001c0028t0001g0364 a0001c0028t0007g0044 others(100): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.3330+3333C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132079 | |||||||
chr1:175132090 | A | G | 199 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(196): Show |
200 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.3330+3344A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132090 | |||||||
chr1:175132098 | T | C | 199 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(196): Show |
200 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.3330+3352T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132098 | |||||||
chr1:175132308 | A | G | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3331-3537A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132308 | |||||||
chr1:175132500 | A | C | 9 | a0001c0001t0001g0093 a0001c0001t0001g0141 a0001c0001t0001g0332 others(6): Show |
9 | HG02486.hp1 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.3331-3345A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132500 | |||||||
chr1:175132555 | C | T | 1 | a0007c0038t0011g0368 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3331-3290C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132555 | |||||||
chr1:175132897 | C | T | 1 | a0022c0027t0001g0198 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3331-2948C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132897 | |||||||
chr1:175132899 | G | C | 1 | a0018c0020t0001g0147 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3331-2946G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132899 | |||||||
chr1:175133025 | G | A | 110 | a0001c0001t0001g0331 a0002c0005t0007g0057 a0002c0009t0001g0049 others(107): Show |
110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.3331-2820G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133025 | |||||||
chr1:175133050 | G | A | 5 | a0002c0005t0004g0009 a0002c0009t0001g0036 a0002c0009t0001g0047 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.3331-2795G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133050 | |||||||
chr1:175133102 | A | G | 305 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.3331-2743A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133102 | |||||||
chr1:175133258 | T | G | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3331-2587T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133258 | |||||||
chr1:175133273 | T | A | 305 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.3331-2572T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133273 | |||||||
chr1:175133603 | C | T | 1 | a0002c0009t0001g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3331-2242C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133603 | |||||||
chr1:175133645 | C | T | 3 | a0001c0016t0001g0360 a0013c0014t0001g0056 a0013c0014t0001g0092 |
3 | HG01358.hp1 HG01517.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3331-2200C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133645 | |||||||
chr1:175133677 | G | A | 4 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(1): Show |
4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-2168G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133677 | |||||||
chr1:175133770 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3331-2075C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133770 | |||||||
chr1:175133869 | G | T | 305 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.3331-1976G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133869 | |||||||
chr1:175133915 | T | C | 4 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(1): Show |
4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-1930T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133915 | |||||||
chr1:175133971 | C | T | 2 | a0021c0056t0006g0274 a0021c0058t0006g0316 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3331-1874C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133971 | |||||||
chr1:175134081 | A | G | 307 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.3331-1764A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134081 | |||||||
chr1:175134416 | G | T | 1 | a0045c0088t0005g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3331-1429G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134416 | |||||||
chr1:175134438 | G | C | 195 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(192): Show |
196 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.3331-1407G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134438 | |||||||
chr1:175134469 | C | T | 1 | a0004c0008t0001g0228 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3331-1376C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134469 | |||||||
chr1:175134475 | G | A | 195 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(192): Show |
196 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.3331-1370G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134475 | |||||||
chr1:175134544 | C | CAA | 189 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(186): Show |
190 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3331-1296_3331-129 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175134544 | ||||||
chr1:175134544 | C | CAAA | 6 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(3): Show |
6 | HG01192.hp2 HG02622.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3331-1297_3331-129 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175134544 | ||||||
chr1:175134551 | C | A | 195 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(192): Show |
196 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.3331-1294C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134551 | |||||||
chr1:175134852 | CT | C | 110 | a0001c0001t0001g0331 a0002c0005t0007g0057 a0002c0009t0001g0049 others(107): Show |
110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.3331-992delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134852 | |||||||
chr1:175134854 | G | A | 3 | a0006c0004t0001g0194 a0006c0004t0001g0195 a0037c0051t0001g0282 |
3 | HG02129.hp1 HG02165.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3331-991G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134854 | |||||||
chr1:175134914 | T | C | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3331-931T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134914 | |||||||
chr1:175134945 | A | T | 4 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(1): Show |
4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-900A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134945 | |||||||
chr1:175134987 | A | AGGACTGA others(5): Show |
1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3331-856_3331-845d others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175134987 | ||||||
chr1:175134987 | A | G | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3331-858A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134987 | |||||||
chr1:175134991 | C | G | 2 | a0021c0056t0006g0274 a0021c0058t0006g0316 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3331-854C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134991 | |||||||
chr1:175135064 | G | A | 4 | a0007c0006t0001g0369 a0007c0006t0015g0011 a0040c0065t0010g0166 others(1): Show |
4 | HG02622.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-781G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135064 | |||||||
chr1:175135091 | T | C | 4 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(1): Show |
4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-754T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135091 | |||||||
chr1:175135117 | G | T | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3331-728G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135117 | |||||||
chr1:175135132 | C | T | 1 | a0011c0011t0001g0240 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3331-713C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135132 | |||||||
chr1:175135384 | AT | A | 4 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(1): Show |
4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-460delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135384 | |||||||
chr1:175135395 | A | G | 1 | a0008c0007t0002g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3331-450A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135395 | |||||||
chr1:175135482 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3331-363A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135482 | |||||||
chr1:175135538 | T | C | 25 | a0002c0005t0001g0142 a0002c0005t0003g0104 a0002c0005t0003g0105 others(22): Show |
25 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.3331-307T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135538 | |||||||
chr1:175135557 | C | G | 25 | a0002c0005t0001g0142 a0002c0005t0003g0104 a0002c0005t0003g0105 others(22): Show |
25 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.3331-288C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135557 | |||||||
chr1:175135583 | T | C | 208 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(205): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.3331-262T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135583 | |||||||
chr1:175135654 | T | C | 99 | a0001c0001t0001g0331 a0002c0005t0007g0057 a0002c0009t0001g0049 others(96): Show |
99 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.3331-191T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135654 | |||||||
chr1:175135660 | G | T | 304 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(301): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.3331-185G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135660 | |||||||
chr1:175135678 | T | C | 4 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(1): Show |
4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-167T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135678 | |||||||
chr1:175136293 | G | A | 1 | a0002c0077t0001g0095 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3427+352G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136293 | |||||||
chr1:175136417 | G | A | 60 | a0003c0015t0001g0312 a0003c0015t0003g0261 a0003c0015t0003g0263 others(57): Show |
60 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.3428-404G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136417 | |||||||
chr1:175136439 | A | G | 9 | a0002c0009t0001g0037 a0002c0009t0001g0038 a0002c0009t0001g0039 others(6): Show |
9 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3428-382A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136439 | |||||||
chr1:175136451 | A | G | 300 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.3428-370A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136451 | |||||||
chr1:175136642 | T | C | 71 | a0001c0001t0001g0165 a0001c0042t0001g0098 a0002c0005t0001g0142 others(68): Show |
71 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(68): Show |
intron_variant | MODIFIER | c.3428-179T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136642 | |||||||
chr1:175136744 | G | A | 229 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.3428-77G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136744 | |||||||
chr1:175136806 | G | A | 368 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(365): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.3428-15G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136806 | |||||||
chr1:175137050 | T | C | 5 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(2): Show |
5 | HG01192.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3595+62T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137050 | |||||||
chr1:175137053 | C | T | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3595+65C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137053 | |||||||
chr1:175137228 | A | G | 9 | a0002c0009t0001g0037 a0002c0009t0001g0038 a0002c0009t0001g0039 others(6): Show |
9 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3595+240A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137228 | |||||||
chr1:175137363 | A | AGT | 10 | a0001c0016t0001g0040 a0002c0005t0002g0019 a0003c0002t0001g0295 others(7): Show |
10 | HG02486.hp2 HG02559.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.3595+403_3595+404d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175137363 | ||||||
chr1:175137363 | A | ATGTGTGT others(6): Show |
1 | a0002c0005t0003g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3595+375_3595+376i others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137363 | |||||||
chr1:175137363 | AGT | A | 51 | a0004c0019t0001g0223 a0005c0003t0001g0169 a0005c0003t0001g0176 others(48): Show |
51 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.3595+403_3595+404d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175137363 | ||||||
chr1:175137363 | AGTGTGTG others(3): Show |
A | 9 | a0002c0009t0001g0037 a0002c0009t0001g0038 a0002c0009t0001g0039 others(6): Show |
9 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3595+395_3595+404d others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175137363 | ||||||
chr1:175137393 | A | T | 234 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.3595+405A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137393 | |||||||
chr1:175137394 | T | G | 234 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.3595+406T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137394 | |||||||
chr1:175137396 | A | G | 235 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3595+408A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137396 | |||||||
chr1:175137397 | T | A | 12 | a0001c0001t0001g0018 a0001c0001t0001g0062 a0001c0016t0001g0356 others(9): Show |
12 | HG00639.hp2 HG01884.hp1 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.3595+409T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | |||||||
chr1:175137397 | T | TGA | 14 | a0001c0001t0001g0332 a0001c0016t0001g0360 a0002c0009t0003g0365 others(11): Show |
14 | HG01517.hp2 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | |||||||
chr1:175137397 | T | TGTGA | 84 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0093 others(81): Show |
85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | |||||||
chr1:175137397 | T | TGTGTGA | 50 | a0001c0001t0001g0031 a0001c0001t0001g0351 a0001c0028t0001g0364 others(47): Show |
50 | HG00408.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | |||||||
chr1:175137397 | T | TGTGTGTG others(1): Show |
17 | a0003c0002t0001g0278 a0003c0002t0001g0292 a0003c0002t0001g0297 others(14): Show |
17 | HG00280.hp1 HG01069.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | |||||||
chr1:175137397 | T | TGTGTGTG others(3): Show |
44 | a0002c0005t0001g0121 a0002c0005t0003g0150 a0003c0002t0001g0266 others(41): Show |
44 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | |||||||
chr1:175137397 | T | TGTGTGTG others(5): Show |
14 | a0001c0001t0001g0331 a0002c0009t0001g0049 a0003c0015t0001g0264 others(11): Show |
14 | HG00099.hp2 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | |||||||
chr1:175137480 | T | C | 97 | a0002c0005t0001g0121 a0003c0002t0001g0266 a0003c0002t0001g0270 others(94): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3595+492T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137480 | |||||||
chr1:175137535 | C | A | 5 | a0001c0031t0005g0063 a0001c0031t0005g0156 a0001c0031t0005g0330 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3595+547C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137535 | |||||||
chr1:175137711 | C | T | 1 | a0041c0094t0001g0308 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3595+723C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137711 | |||||||
chr1:175137723 | T | C | 235 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3595+735T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137723 | |||||||
chr1:175137739 | AGTGTTTT others(11): Show |
A | 3 | a0017c0025t0001g0081 a0017c0025t0001g0097 a0056c0052t0001g0231 |
3 | NA18955.hp1 NA19060.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.3595+768_3595+785d others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175137739 | ||||||
chr1:175137804 | T | C | 3 | a0001c0016t0001g0360 a0013c0014t0001g0056 a0013c0014t0001g0092 |
3 | HG01358.hp1 HG01517.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3595+816T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137804 | |||||||
chr1:175137865 | A | C | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3595+877A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137865 | |||||||
chr1:175137990 | C | A | 1 | a0008c0007t0002g0134 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3595+1002C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137990 | |||||||
chr1:175138050 | G | A | 1 | a0006c0004t0001g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3595+1062G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138050 | |||||||
chr1:175138060 | G | T | 4 | a0002c0005t0002g0019 a0002c0005t0002g0022 a0004c0008t0002g0199 others(1): Show |
4 | NA18944.hp1 NA18957.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3595+1072G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138060 | |||||||
chr1:175138068 | G | T | 5 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(2): Show |
5 | HG01192.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3595+1080G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138068 | |||||||
chr1:175138128 | T | C | 235 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3595+1140T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138128 | |||||||
chr1:175138250 | A | C | 5 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(2): Show |
5 | HG01192.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3595+1262A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138250 | |||||||
chr1:175138365 | A | G | 102 | a0001c0001t0001g0331 a0002c0005t0001g0121 a0002c0009t0001g0049 others(99): Show |
102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3595+1377A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138365 | |||||||
chr1:175138458 | T | C | 5 | a0007c0006t0001g0337 a0007c0006t0001g0369 a0007c0006t0001g0370 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3595+1470T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138458 | |||||||
chr1:175138621 | A | G | 2 | a0007c0006t0001g0084 a0021c0057t0001g0175 |
2 | HG01069.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3595+1633A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138621 | |||||||
chr1:175138690 | C | T | 86 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(83): Show |
87 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.3595+1702C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138690 | |||||||
chr1:175138735 | G | T | 2 | a0010c0010t0001g0110 a0010c0010t0001g0112 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3595+1747G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138735 | |||||||
chr1:175139274 | G | A | 51 | a0004c0019t0001g0223 a0005c0003t0001g0169 a0005c0003t0001g0176 others(48): Show |
51 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.3595+2286G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139274 | |||||||
chr1:175139493 | G | T | 235 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3595+2505G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139493 | |||||||
chr1:175139614 | G | A | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3595+2626G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139614 | |||||||
chr1:175139615 | A | AT | 232 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.3595+2636dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175139615 | ||||||
chr1:175139696 | A | G | 235 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3595+2708A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139696 | |||||||
chr1:175139883 | C | T | 1 | a0002c0005t0002g0346 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3595+2895C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139883 | |||||||
chr1:175139911 | T | C | 6 | a0002c0029t0001g0055 a0007c0006t0001g0006 a0007c0006t0001g0007 others(3): Show |
6 | HG02809.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3595+2923T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139911 | |||||||
chr1:175139917 | T | C | 1 | a0035c0063t0001g0268 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3595+2929T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139917 | |||||||
chr1:175140066 | G | A | 1 | a0004c0019t0001g0353 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3595+3078G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140066 | |||||||
chr1:175140266 | A | G | 9 | a0002c0009t0001g0037 a0002c0009t0001g0038 a0002c0009t0001g0039 others(6): Show |
9 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3595+3278A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140266 | |||||||
chr1:175140356 | T | G | 102 | a0001c0001t0001g0331 a0002c0005t0001g0121 a0002c0009t0001g0049 others(99): Show |
102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3595+3368T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140356 | |||||||
chr1:175140364 | G | T | 51 | a0004c0019t0001g0223 a0005c0003t0001g0169 a0005c0003t0001g0176 others(48): Show |
51 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.3595+3376G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140364 | |||||||
chr1:175140381 | G | A | 102 | a0001c0001t0001g0331 a0002c0005t0001g0121 a0002c0009t0001g0049 others(99): Show |
102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3595+3393G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140381 | |||||||
chr1:175140491 | C | G | 77 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(74): Show |
78 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.3595+3503C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140491 | |||||||
chr1:175140586 | A | G | 245 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.3595+3598A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140586 | |||||||
chr1:175140703 | T | G | 1 | a0011c0011t0003g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3596-3684T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140703 | |||||||
chr1:175140748 | C | T | 50 | a0004c0019t0001g0223 a0005c0003t0001g0169 a0005c0003t0001g0176 others(47): Show |
50 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.3596-3639C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140748 | |||||||
chr1:175140780 | C | T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0141 a0001c0001t0001g0332 others(6): Show |
9 | HG02486.hp1 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.3596-3607C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140780 | |||||||
chr1:175140795 | A | G | 1 | a0042c0071t0004g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3596-3592A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140795 | |||||||
chr1:175140837 | T | C | 2 | a0027c0039t0009g0010 a0027c0039t0009g0012 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3596-3550T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140837 | |||||||
chr1:175141027 | G | A | 34 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(31): Show |
35 | HG00099.hp1 HG00544.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.3596-3360G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141027 | |||||||
chr1:175141055 | G | T | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3596-3332G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141055 | |||||||
chr1:175141121 | A | C | 2 | a0027c0039t0009g0010 a0027c0039t0009g0012 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3596-3266A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141121 | |||||||
chr1:175141210 | G | A | 1 | a0042c0071t0004g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3596-3177G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141210 | |||||||
chr1:175141344 | C | T | 101 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(98): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.3596-3043C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141344 | |||||||
chr1:175141381 | C | T | 2 | a0040c0065t0010g0166 a0045c0088t0005g0102 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3596-3006C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141381 | |||||||
chr1:175141763 | C | A | 1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3596-2624C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141763 | |||||||
chr1:175141816 | C | T | 2 | a0027c0039t0009g0010 a0027c0039t0009g0012 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3596-2571C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141816 | |||||||
chr1:175141819 | C | A | 96 | a0001c0001t0002g0122 a0001c0001t0002g0163 a0001c0016t0001g0040 others(93): Show |
98 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.3596-2568C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141819 | |||||||
chr1:175141898 | A | G | 1 | a0006c0004t0001g0253 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3596-2489A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141898 | |||||||
chr1:175141964 | C | A | 1 | a0004c0019t0001g0209 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3596-2423C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141964 | |||||||
chr1:175142217 | C | T | 3 | a0001c0001t0001g0020 a0002c0005t0003g0150 a0009c0012t0003g0273 |
3 | HG01109.hp2 HG02071.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3596-2170C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142217 | |||||||
chr1:175142233 | G | A | 33 | a0002c0005t0003g0104 a0002c0005t0003g0105 a0002c0005t0003g0106 others(30): Show |
33 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.3596-2154G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142233 | |||||||
chr1:175142269 | C | T | 1 | a0002c0009t0003g0359 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3596-2118C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142269 | |||||||
chr1:175142398 | C | CTTATTTT others(52): Show |
1 | a0004c0008t0002g0225 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3596-1950_3596-194 others(63): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175142398 | ||||||
chr1:175142438 | C | T | 367 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(364): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.3596-1949C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142438 | |||||||
chr1:175142470 | C | CAAAT | 263 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(260): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.3596-1915_3596-191 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175142470 | ||||||
chr1:175142499 | C | T | 5 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(2): Show |
5 | HG01192.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3596-1888C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142499 | |||||||
chr1:175142512 | G | A | 1 | a0027c0039t0009g0012 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3596-1875G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142512 | |||||||
chr1:175142624 | C | CT | 88 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(85): Show |
89 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3596-1752dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175142624 | ||||||
chr1:175142711 | G | A | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3596-1676G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142711 | |||||||
chr1:175142782 | C | T | 364 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(361): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.3596-1605C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142782 | |||||||
chr1:175142806 | C | T | 3 | a0009c0021t0001g0004 a0022c0027t0001g0218 a0022c0027t0001g0222 |
3 | HG00639.hp1 HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3596-1581C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142806 | |||||||
chr1:175142810 | G | A | 100 | a0001c0001t0001g0331 a0002c0005t0001g0114 a0002c0009t0001g0049 others(97): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.3596-1577G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142810 | |||||||
chr1:175142817 | C | T | 263 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(260): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.3596-1570C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142817 | |||||||
chr1:175142905 | C | G | 4 | a0005c0003t0001g0255 a0018c0020t0001g0066 a0018c0020t0001g0068 others(1): Show |
4 | NA18956.hp2 NA18989.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.3596-1482C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142905 | |||||||
chr1:175142962 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3596-1425C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142962 | |||||||
chr1:175143026 | C | T | 2 | a0004c0019t0001g0353 a0006c0004t0001g0244 |
2 | HG01346.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.3596-1361C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175143026 | |||||||
chr1:175143182 | C | T | 3 | a0001c0016t0001g0040 a0038c0085t0001g0335 a0057c0078t0001g0164 |
3 | HG02145.hp2 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3596-1205C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175143182 | |||||||
chr1:175143228 | TGAGATGA others(52): Show |
T | 1 | a0004c0008t0002g0225 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3596-1156_3596-109 others(63): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143228 | ||||||
chr1:175143518 | G | GGTGT | 10 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(7): Show |
10 | HG01192.hp2 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.3596-852_3596-849d others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | ||||||
chr1:175143518 | G | GGTGTGT | 46 | a0001c0016t0001g0040 a0002c0005t0003g0104 a0002c0005t0003g0105 others(43): Show |
47 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.3596-854_3596-849d others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | ||||||
chr1:175143518 | G | GGTGTGTG others(1): Show |
140 | a0001c0001t0001g0331 a0001c0042t0001g0098 a0002c0005t0001g0114 others(137): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.3596-856_3596-849d others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | ||||||
chr1:175143518 | G | GGTGTGTG others(3): Show |
20 | a0002c0009t0001g0041 a0003c0002t0001g0266 a0005c0003t0001g0180 others(17): Show |
20 | HG01433.hp1 HG01978.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.3596-858_3596-849d others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | ||||||
chr1:175143518 | G | GGTGTGTG others(5): Show |
92 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0031 others(89): Show |
93 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.3596-860_3596-849d others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | ||||||
chr1:175143518 | G | GGTGTGTG others(7): Show |
4 | a0001c0087t0001g0024 a0007c0006t0015g0011 a0013c0014t0001g0092 others(1): Show |
4 | HG03130.hp2 HG03927.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.3596-862_3596-849d others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | ||||||
chr1:175143531 | G | GTGTT | 51 | a0001c0001t0002g0122 a0001c0001t0002g0163 a0002c0005t0002g0019 others(48): Show |
52 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.3596-853_3596-852i others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143531 | ||||||
chr1:175143608 | G | C | 1 | a0003c0002t0001g0283 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3596-779G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175143608 | |||||||
chr1:175143622 | T | G | 3 | a0002c0005t0002g0347 a0004c0008t0002g0206 a0009c0012t0002g0326 |
3 | HG02135.hp2 HG02523.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3596-765T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175143622 | |||||||
chr1:175143931 | GTA | G | 160 | a0001c0001t0001g0331 a0001c0042t0001g0098 a0002c0005t0001g0114 others(157): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.3596-454_3596-453d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143931 | ||||||
chr1:175143982 | T | G | 263 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(260): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.3596-405T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175143982 | |||||||
chr1:175144048 | T | G | 364 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(361): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.3596-339T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175144048 | |||||||
chr1:175144114 | A | C | 5 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(2): Show |
5 | HG01192.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3596-273A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175144114 | |||||||
chr1:175144228 | TC | T | 3 | a0002c0009t0001g0042 a0002c0009t0001g0043 a0002c0009t0013g0048 |
3 | HG02257.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3596-156delC | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175144228 | ||||||
chr1:175144369 | G | A | 1 | a0005c0003t0001g0200 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3596-18G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175144369 | |||||||
chr1:175144879 | T | C | 35 | a0002c0005t0003g0104 a0002c0005t0003g0105 a0002c0005t0003g0106 others(32): Show |
35 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.3759+329T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175144879 | |||||||
chr1:175145062 | A | T | 2 | a0007c0006t0001g0084 a0021c0057t0001g0175 |
2 | HG01069.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3759+512A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145062 | |||||||
chr1:175145156 | G | T | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3759+606G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145156 | |||||||
chr1:175145337 | G | A | 263 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(260): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.3759+787G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145337 | |||||||
chr1:175145539 | C | A | 262 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(259): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.3759+989C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145539 | |||||||
chr1:175145552 | C | CA | 8 | a0002c0005t0003g0149 a0003c0015t0003g0267 a0004c0008t0003g0246 others(5): Show |
8 | HG00609.hp2 HG01109.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.3759+1025dupA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145552 | C | CAAAAAA | 74 | a0001c0001t0001g0331 a0002c0005t0001g0114 a0002c0009t0001g0049 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.3759+1020_3759+102 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145552 | C | CAAAAAAA | 25 | a0001c0028t0001g0364 a0001c0028t0007g0044 a0001c0028t0007g0046 others(22): Show |
25 | HG00438.hp2 HG00738.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.3759+1019_3759+102 others(11): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145552 | C | CAAAAAAA others(2): Show |
44 | a0002c0005t0001g0121 a0002c0009t0001g0041 a0003c0002t0001g0286 others(41): Show |
44 | HG00323.hp2 HG01243.hp1 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.3759+1017_3759+102 others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145552 | C | CAAAAAAA others(3): Show |
13 | a0001c0042t0001g0098 a0005c0003t0001g0176 a0005c0003t0001g0188 others(10): Show |
13 | HG01243.hp2 HG01928.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.3759+1016_3759+102 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145552 | C | CAAAAAAA others(4): Show |
6 | a0015c0024t0001g0371 a0017c0025t0001g0081 a0018c0020t0001g0147 others(3): Show |
6 | HG00642.hp2 HG03139.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3759+1015_3759+102 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145552 | C | CAAAAAAA others(5): Show |
4 | a0003c0002t0012g0277 a0011c0011t0001g0197 a0011c0011t0001g0238 others(1): Show |
4 | HG00408.hp1 HG02698.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3759+1014_3759+102 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145552 | C | CAAAAAAA others(6): Show |
6 | a0001c0001t0001g0333 a0001c0016t0001g0362 a0002c0009t0001g0038 others(3): Show |
6 | HG01261.hp2 HG01358.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3759+1013_3759+102 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145552 | C | CAAAAAAA others(7): Show |
34 | a0001c0001t0001g0018 a0001c0001t0001g0062 a0001c0001t0001g0107 others(31): Show |
35 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.3759+1012_3759+102 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145552 | C | CAAAAAAA others(8): Show |
43 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0031 others(40): Show |
43 | HG00544.hp1 HG00738.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.3759+1011_3759+102 others(19): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145552 | C | CAAAAAAA others(9): Show |
11 | a0001c0001t0001g0093 a0001c0001t0001g0123 a0001c0001t0001g0141 others(8): Show |
11 | HG01081.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3759+1010_3759+102 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | ||||||
chr1:175145675 | A | T | 3 | a0001c0001t0001g0334 a0001c0042t0001g0082 a0019c0023t0001g0241 |
3 | HG02486.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3759+1125A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145675 | |||||||
chr1:175145700 | G | T | 1 | a0007c0006t0001g0153 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3759+1150G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145700 | |||||||
chr1:175145769 | C | T | 4 | a0003c0002t0001g0300 a0007c0006t0001g0115 a0007c0006t0001g0118 others(1): Show |
4 | NA18945.hp2 NA18999.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.3760-1162C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145769 | |||||||
chr1:175145770 | G | A | 61 | a0001c0001t0002g0122 a0001c0001t0002g0163 a0001c0016t0001g0040 others(58): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.3760-1161G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145770 | |||||||
chr1:175145806 | C | T | 2 | a0007c0006t0001g0006 a0007c0006t0001g0007 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3760-1125C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145806 | |||||||
chr1:175145912 | G | C | 364 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(361): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.3760-1019G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145912 | |||||||
chr1:175146124 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0141 a0001c0073t0001g0052 |
3 | HG02572.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3760-807C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175146124 | |||||||
chr1:175146233 | CCTGAACC others(12): Show |
C | 1 | a0012c0013t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3760-695_3760-677d others(21): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175146233 | ||||||
chr1:175146431 | A | C | 258 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(255): Show |
259 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3760-500A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175146431 | |||||||
chr1:175146603 | G | A | 5 | a0001c0031t0005g0063 a0001c0031t0005g0156 a0001c0031t0005g0330 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3760-328G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175146603 | |||||||
chr1:175146646 | A | G | 1 | a0020c0022t0001g0289 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3760-285A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175146646 | |||||||
chr1:175146729 | C | G | 3 | a0002c0005t0002g0019 a0002c0005t0002g0022 a0004c0008t0002g0199 |
3 | NA18944.hp1 NA18957.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.3760-202C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175146729 | |||||||
chr1:175146910 | C | CT | 262 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(259): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
splice_region_variant&intron_variant | LOW | c.3760-6dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175146910 |