Item | Value |
---|---|
geneid | 10206 |
ensemblid | ENSG00000204977.10 |
hgncid | 9976 |
symbol | TRIM13 |
name | tripartite motif containing 13 |
refseq_nuc | NM_213590.3 |
refseq_prot | NP_998755.1 |
ensembl_nuc | ENST00000378182.4 |
ensembl_prot | ENSP00000367424.3 |
mane_status | MANE Select |
chr | chr13 |
start | 49997042 |
end | 50018467 |
strand | + |
ver | v1.2 |
region | chr13:49997042-50018467 |
region5000 | chr13:49992042-50023467 |
regionname0 | TRIM13_chr13_49997042_50018467 |
regionname5000 | TRIM13_chr13_49992042_50023467 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 407 | 376 | 87 | 62 | 161 | 16 | 48 | 117 | TRIM13_chr13_49992042_50023467 | TRIM13 | MELLE others(402): Show |
chr13 | 49992042 | 50023467 |
a0002 | 0/0 | 407 | 11 | 7 | 4 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | MELLE others(402): Show |
chr13 | 49992042 | 50023467 |
a0003 | 0/0 | 407 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | MELLE others(402): Show |
chr13 | 49992042 | 50023467 |
a0004 | 0/0 | 407 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | MELLE others(402): Show |
chr13 | 49992042 | 50023467 |
a0005 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | MELLE others(402): Show |
chr13 | 49992042 | 50023467 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1221 | 373 | 84 | 62 | 161 | 16 | 48 | TRIM13_chr13_49992042_50023467 | TRIM13 | ATGGA others(1216): Show |
chr13 | 49992042 | 50023467 | ||
a0001c0003 | 0/0 | 1221 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | ATGGA others(1216): Show |
chr13 | 49992042 | 50023467 | ||
a0002c0002 | 0/0 | 1221 | 11 | 7 | 4 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | ATGGA others(1216): Show |
chr13 | 49992042 | 50023467 | ||
a0003c0006 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | ATGGA others(1216): Show |
chr13 | 49992042 | 50023467 | ||
a0004c0004 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | ATGGA others(1216): Show |
chr13 | 49992042 | 50023467 | ||
a0005c0005 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | ATGGA others(1216): Show |
chr13 | 49992042 | 50023467 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7261 | 14 | 0 | 4 | 8 | 2 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0002 | 0/0 | 7257 | 14 | 0 | 4 | 9 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0003 | 0/0 | 7254 | 11 | 1 | 1 | 7 | 0 | 2 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0004 | 0/0 | 7253 | 10 | 4 | 3 | 0 | 3 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0005 | 0/0 | 7263 | 10 | 0 | 0 | 9 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7258): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0006 | 0/0 | 7253 | 9 | 0 | 0 | 9 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0007 | 0/0 | 7261 | 8 | 0 | 0 | 8 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0008 | 0/0 | 7267 | 7 | 1 | 3 | 2 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7262): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0009 | 0/0 | 7251 | 7 | 0 | 5 | 0 | 0 | 2 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7246): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0010 | 0/0 | 7257 | 7 | 0 | 6 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0011 | 0/0 | 7261 | 6 | 0 | 1 | 3 | 0 | 2 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0012 | 0/0 | 7268 | 6 | 0 | 0 | 5 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7263): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0013 | 1/0 | 7255 | 6 | 4 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0014 | 0/0 | 7254 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0015 | 0/0 | 7253 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0016 | 0/0 | 7261 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0017 | 0/0 | 7253 | 5 | 0 | 0 | 2 | 0 | 3 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0018 | 0/0 | 7254 | 5 | 0 | 0 | 4 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0019 | 0/0 | 7269 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7264): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0020 | 0/0 | 7250 | 4 | 1 | 0 | 0 | 2 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7245): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0021 | 0/0 | 7257 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0022 | 0/0 | 7256 | 3 | 0 | 0 | 1 | 0 | 2 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7251): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0023 | 0/0 | 7253 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0024 | 0/0 | 7253 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0025 | 0/0 | 7253 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0026 | 0/0 | 7259 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7254): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0027 | 0/0 | 7253 | 3 | 1 | 0 | 1 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0028 | 0/0 | 7253 | 3 | 0 | 1 | 0 | 0 | 2 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0029 | 0/0 | 7265 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7260): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0030 | 0/0 | 7263 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7258): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0031 | 0/0 | 7253 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0032 | 0/0 | 7271 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7266): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0033 | 0/0 | 7268 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7263): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0034 | 0/0 | 7255 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0035 | 0/0 | 7270 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7265): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0036 | 0/0 | 7255 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0037 | 0/0 | 7268 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7263): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0038 | 0/0 | 7259 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7254): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0039 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0040 | 0/0 | 7259 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7254): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0041 | 0/0 | 7253 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0042 | 0/0 | 7253 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0043 | 0/0 | 7267 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7262): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0044 | 0/0 | 7258 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7253): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0045 | 0/0 | 7262 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7257): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0046 | 0/0 | 7253 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0047 | 0/0 | 7269 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7264): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0048 | 0/0 | 7252 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0049 | 0/0 | 7251 | 2 | 1 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7246): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0050 | 0/0 | 7268 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7263): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0051 | 0/0 | 7269 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7264): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0052 | 0/0 | 7255 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0053 | 0/0 | 7256 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7251): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0055 | 0/0 | 7254 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0056 | 0/0 | 7254 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0057 | 0/0 | 7255 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0058 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0059 | 0/0 | 7262 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7257): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0060 | 0/0 | 7262 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7257): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0061 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7259): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0062 | 0/0 | 7268 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7263): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0064 | 0/0 | 7254 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0065 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0066 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0067 | 0/0 | 7262 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7257): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0068 | 0/0 | 7258 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7253): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0069 | 0/0 | 7256 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7251): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0070 | 0/0 | 7252 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0072 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7259): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0073 | 0/0 | 7257 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0074 | 0/0 | 7252 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0075 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7257): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0076 | 0/0 | 7253 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0077 | 0/0 | 7255 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0078 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0079 | 0/0 | 7257 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0080 | 0/0 | 7257 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0081 | 0/0 | 7256 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7251): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0083 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7246): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0084 | 0/0 | 7260 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7255): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0085 | 0/0 | 7252 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0086 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0087 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0088 | 0/0 | 7254 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0089 | 0/0 | 7253 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0090 | 0/0 | 7253 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0091 | 0/0 | 7252 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0092 | 0/0 | 7248 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7243): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0093 | 0/0 | 7263 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7258): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0094 | 0/0 | 7261 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0095 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0096 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0097 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0098 | 0/0 | 7257 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0099 | 0/0 | 7257 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0100 | 0/0 | 7257 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0101 | 0/0 | 7257 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0102 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0103 | 0/0 | 7254 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0104 | 0/0 | 7253 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0105 | 0/0 | 7253 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0106 | 0/0 | 7253 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0107 | 0/0 | 7253 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0108 | 0/0 | 7262 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7257): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0109 | 0/0 | 7267 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7262): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0110 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7260): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0111 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7260): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0112 | 0/0 | 7258 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7253): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0113 | 0/0 | 7262 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7257): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0114 | 0/0 | 7260 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7255): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0115 | 0/0 | 7271 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7266): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0117 | 0/0 | 7267 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7262): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0118 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7260): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0119 | 0/0 | 7260 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7255): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0120 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0121 | 0/0 | 7257 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0122 | 0/0 | 7253 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0123 | 0/0 | 7253 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0124 | 0/0 | 7269 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7264): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0125 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7260): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0126 | 0/0 | 7263 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7258): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0127 | 0/0 | 7263 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7258): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0128 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7260): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0129 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7259): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0130 | 0/1 | 7223 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7218): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0131 | 0/0 | 7252 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0132 | 0/0 | 7252 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0133 | 0/0 | 7268 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7263): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0134 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7259): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0135 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7245): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0136 | 0/0 | 7255 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0137 | 0/0 | 7267 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7262): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0138 | 0/0 | 7269 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7264): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0139 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7268): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0140 | 0/0 | 7275 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7270): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0141 | 0/0 | 7252 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0142 | 0/0 | 7252 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0143 | 0/0 | 7256 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7251): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0144 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7245): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0145 | 0/0 | 7252 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0146 | 0/0 | 7253 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0147 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7245): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0148 | 0/0 | 7251 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7246): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0149 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0150 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0151 | 0/0 | 7251 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7246): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0152 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0153 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0154 | 0/0 | 7258 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7253): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0155 | 0/0 | 7258 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7253): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0156 | 0/0 | 7254 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0157 | 0/0 | 7253 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0158 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7246): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0159 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7259): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0160 | 0/0 | 7262 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7257): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0161 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7259): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0162 | 0/0 | 7264 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7259): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0163 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0164 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0167 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0168 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0170 | 0/0 | 7252 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0173 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0174 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0178 | 0/0 | 7256 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7251): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0179 | 0/0 | 7246 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7241): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0180 | 0/0 | 7253 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0181 | 0/0 | 7253 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0182 | 0/0 | 7256 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7251): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0183 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0184 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0185 | 0/0 | 7254 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0186 | 0/0 | 7258 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7253): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0187 | 0/0 | 7267 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7262): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0188 | 0/0 | 7269 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7264): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0189 | 0/0 | 7251 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7246): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0190 | 0/0 | 7271 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7266): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0191 | 0/0 | 7254 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0192 | 0/0 | 7253 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0193 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0194 | 0/0 | 7258 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7253): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0195 | 0/0 | 7258 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7253): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0196 | 0/0 | 7255 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0197 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0198 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0199 | 0/0 | 7255 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0200 | 0/0 | 7219 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7214): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0201 | 0/0 | 7257 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7252): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0202 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0203 | 0/0 | 7258 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7253): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0204 | 0/0 | 7253 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7248): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0205 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0206 | 0/0 | 7255 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0207 | 0/0 | 7254 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0001c0001t0208 | 0/0 | 7255 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7250): Show |
chr13 | 49992042 | 50023467 |
a0001c0003t0039 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7256): Show |
chr13 | 49992042 | 50023467 |
a0001c0003t0071 | 0/0 | 7266 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7261): Show |
chr13 | 49992042 | 50023467 |
a0001c0003t0116 | 0/0 | 7267 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7262): Show |
chr13 | 49992042 | 50023467 |
a0002c0002t0054 | 0/0 | 7267 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7262): Show |
chr13 | 49992042 | 50023467 |
a0002c0002t0063 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7276): Show |
chr13 | 49992042 | 50023467 |
a0002c0002t0165 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7275): Show |
chr13 | 49992042 | 50023467 |
a0002c0002t0166 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7276): Show |
chr13 | 49992042 | 50023467 |
a0002c0002t0169 | 0/0 | 7272 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7267): Show |
chr13 | 49992042 | 50023467 |
a0002c0002t0171 | 0/0 | 7281 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7276): Show |
chr13 | 49992042 | 50023467 |
a0002c0002t0172 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7260): Show |
chr13 | 49992042 | 50023467 |
a0002c0002t0175 | 0/0 | 7258 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7253): Show |
chr13 | 49992042 | 50023467 |
a0002c0002t0176 | 0/0 | 7266 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7261): Show |
chr13 | 49992042 | 50023467 |
a0002c0002t0177 | 0/0 | 7273 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7268): Show |
chr13 | 49992042 | 50023467 |
a0003c0006t0082 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7249): Show |
chr13 | 49992042 | 50023467 |
a0004c0004t0048 | 0/0 | 7252 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7247): Show |
chr13 | 49992042 | 50023467 |
a0005c0005t0029 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | GAGTC others(7260): Show |
chr13 | 49992042 | 50023467 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 3 | 3 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0003g0003 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0004g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0005g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0005g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0006g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0006g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0007g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0007g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0008g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0008g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0009g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0009g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0009g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0009g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0009g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0010g0005 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0010g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0011g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0011g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0011g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0011g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0012g0001 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0012g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0013g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0013g0029 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0013g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0013g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0014g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0014g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0014g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0014g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0015g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0015g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0015g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0015g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0015g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0016g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0016g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0016g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0016g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0016g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0017g0002 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0017g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0018g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0018g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0018g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0019g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0019g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0019g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0019g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0020g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0020g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0020g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0021g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0021g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0021g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0022g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0022g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0023g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0023g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0023g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0024g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0024g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0024g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0025g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0025g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0025g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0026g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0026g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0026g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0027g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0027g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0027g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0028g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0028g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0028g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0029g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0029g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0030g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0030g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0030g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0031g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0031g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0032g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0032g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0032g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0033g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0033g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0034g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0034g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0035g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0035g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0035g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0036g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0036g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0037g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0037g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0038g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0038g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0039g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0040g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0040g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0041g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0042g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0042g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0043g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0043g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0044g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0044g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0045g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0046g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0046g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0047g0001 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0048g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0049g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0049g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0050g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0050g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0051g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0051g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0052g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0053g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0055g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0055g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0056g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0057g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0058g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0059g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0060g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0061g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0062g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0064g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0065g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0066g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0067g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0068g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0069g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0070g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0072g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0073g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0074g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0075g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0076g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0077g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0078g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0079g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0080g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0081g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0083g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0084g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0085g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0086g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0087g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0088g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0089g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0090g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0091g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0092g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0093g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0094g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0095g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0096g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0097g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0098g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0099g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0100g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0101g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0102g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0103g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0104g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0105g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0106g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0107g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0108g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0109g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0110g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0111g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0112g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0113g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0114g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0115g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0117g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0118g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0119g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0120g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0121g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0122g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0123g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0124g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0125g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0126g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0127g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0128g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0129g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0130g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0131g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0132g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0133g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0134g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0135g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0136g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0137g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0138g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0139g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0140g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0141g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0142g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0143g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0144g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0145g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0146g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0147g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0148g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0149g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0150g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0151g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0152g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0153g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0154g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0155g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0156g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0157g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0158g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0159g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0160g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0161g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0162g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0163g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0164g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0167g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0168g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0170g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0173g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0174g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0178g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0179g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0180g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0181g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0182g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0183g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0184g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0185g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0186g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0187g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0188g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0189g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0190g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0191g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0192g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0193g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0194g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0195g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0196g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0197g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0198g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0199g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0200g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0201g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0202g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0203g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0204g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0205g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0206g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0207g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0001t0208g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0003t0039g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0003t0071g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0001c0003t0116g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0002c0002t0054g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0002c0002t0063g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0002c0002t0165g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0002c0002t0166g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0002c0002t0169g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0002c0002t0171g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0002c0002t0172g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0002c0002t0175g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0002c0002t0176g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0002c0002t0177g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0003c0006t0082g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0004c0004t0048g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
a0005c0005t0029g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0089 | g0006 | EUR | GBR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00099 | hp2 | a0001 | c0001 | t0012 | g0001 | EUR | GBR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00140 | hp1 | a0001 | c0001 | t0049 | g0002 | EUR | GBR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00140 | hp2 | a0001 | c0001 | t0103 | g0001 | EUR | GBR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00323 | hp1 | a0001 | c0001 | t0146 | g0001 | EUR | FIN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00323 | hp2 | a0001 | c0001 | t0070 | g0063 | EUR | FIN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00408 | hp1 | a0001 | c0001 | t0099 | g0008 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00423 | hp1 | a0001 | c0001 | t0206 | g0017 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00423 | hp2 | a0001 | c0001 | t0112 | g0043 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00544 | hp1 | a0001 | c0001 | t0097 | g0122 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00544 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00558 | hp1 | a0001 | c0001 | t0006 | g0136 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00558 | hp2 | a0001 | c0001 | t0016 | g0135 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00597 | hp1 | a0001 | c0001 | t0111 | g0046 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00609 | hp1 | a0001 | c0001 | t0019 | g0174 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00609 | hp2 | a0001 | c0001 | t0119 | g0111 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00621 | hp1 | a0001 | c0001 | t0125 | g0007 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00621 | hp2 | a0001 | c0001 | t0011 | g0126 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00639 | hp1 | a0001 | c0001 | t0143 | g0003 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00733 | hp1 | a0001 | c0001 | t0010 | g0005 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00733 | hp2 | a0001 | c0001 | t0180 | g0066 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00735 | hp1 | a0001 | c0001 | t0046 | g0080 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00735 | hp2 | a0001 | c0001 | t0132 | g0002 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00738 | hp1 | a0001 | c0001 | t0010 | g0005 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00741 | hp1 | a0001 | c0001 | t0011 | g0038 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG00741 | hp2 | a0001 | c0001 | t0187 | g0045 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01069 | hp1 | a0001 | c0001 | t0156 | g0058 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01069 | hp2 | a0001 | c0001 | t0010 | g0005 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01074 | hp1 | a0001 | c0001 | t0013 | g0021 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01074 | hp2 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01081 | hp1 | a0001 | c0001 | t0088 | g0006 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01081 | hp2 | a0001 | c0001 | t0040 | g0013 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01099 | hp1 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01099 | hp2 | a0001 | c0001 | t0010 | g0005 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0028 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01106 | hp2 | a0001 | c0001 | t0021 | g0031 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01109 | hp1 | a0002 | c0002 | t0176 | g0048 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01109 | hp2 | a0002 | c0002 | t0171 | g0184 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01167 | hp1 | a0001 | c0001 | t0109 | g0001 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01167 | hp2 | a0002 | c0002 | t0054 | g0050 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01168 | hp2 | a0001 | c0001 | t0041 | g0006 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01169 | hp1 | a0002 | c0002 | t0054 | g0050 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01169 | hp2 | a0001 | c0001 | t0041 | g0006 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01175 | hp1 | a0001 | c0001 | t0181 | g0006 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01175 | hp2 | a0001 | c0001 | t0050 | g0026 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01192 | hp1 | a0001 | c0001 | t0189 | g0073 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01192 | hp2 | a0001 | c0001 | t0192 | g0185 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01243 | hp2 | a0001 | c0001 | t0182 | g0009 | AMR | PUR | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01255 | hp1 | a0001 | c0001 | t0045 | g0016 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01256 | hp1 | a0001 | c0001 | t0090 | g0032 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01256 | hp2 | a0001 | c0001 | t0026 | g0040 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01358 | hp1 | a0001 | c0001 | t0008 | g0012 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01358 | hp2 | a0001 | c0001 | t0031 | g0077 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01361 | hp1 | a0001 | c0001 | t0026 | g0128 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01361 | hp2 | a0001 | c0001 | t0009 | g0079 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0062 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01496 | hp1 | a0001 | c0001 | t0199 | g0005 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01496 | hp2 | a0001 | c0001 | t0138 | g0001 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0071 | EUR | IBS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0068 | EUR | IBS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01516 | hp2 | a0001 | c0001 | t0027 | g0098 | EUR | IBS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01517 | hp1 | a0001 | c0001 | t0047 | g0001 | EUR | IBS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0064 | EUR | IBS | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01884 | hp1 | a0001 | c0001 | t0036 | g0009 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01884 | hp2 | a0001 | c0001 | t0144 | g0110 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01891 | hp1 | a0001 | c0001 | t0015 | g0145 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01891 | hp2 | a0001 | c0001 | t0013 | g0092 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01934 | hp1 | a0001 | c0001 | t0160 | g0010 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01934 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01975 | hp2 | a0001 | c0001 | t0031 | g0002 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01978 | hp1 | a0001 | c0001 | t0028 | g0006 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01981 | hp1 | a0001 | c0001 | t0093 | g0001 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01981 | hp2 | a0001 | c0001 | t0045 | g0016 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01993 | hp1 | a0001 | c0001 | t0009 | g0084 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01993 | hp2 | a0001 | c0001 | t0191 | g0028 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02004 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02015 | hp1 | a0001 | c0001 | t0102 | g0010 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02015 | hp2 | a0001 | c0001 | t0091 | g0139 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02027 | hp1 | a0001 | c0001 | t0157 | g0153 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02027 | hp2 | a0001 | c0001 | t0051 | g0001 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02040 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02040 | hp2 | a0001 | c0001 | t0100 | g0008 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02055 | hp1 | a0001 | c0001 | t0013 | g0029 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02055 | hp2 | a0001 | c0001 | t0008 | g0168 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02056 | hp1 | a0001 | c0001 | t0058 | g0011 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02056 | hp2 | a0001 | c0001 | t0086 | g0144 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02071 | hp1 | a0001 | c0001 | t0055 | g0011 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02074 | hp1 | a0001 | c0001 | t0159 | g0155 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02074 | hp2 | a0001 | c0001 | t0035 | g0013 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02080 | hp1 | a0001 | c0001 | t0158 | g0154 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02080 | hp2 | a0001 | c0001 | t0016 | g0164 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02083 | hp1 | a0001 | c0001 | t0022 | g0003 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02135 | hp1 | a0001 | c0001 | t0101 | g0026 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02135 | hp2 | a0001 | c0001 | t0030 | g0160 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02145 | hp1 | a0002 | c0002 | t0063 | g0193 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02145 | hp2 | a0001 | c0001 | t0013 | g0051 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02148 | hp1 | a0001 | c0001 | t0050 | g0013 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | CDX | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02155 | hp2 | a0001 | c0001 | t0140 | g0001 | EAS | CDX | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02165 | hp1 | a0001 | c0001 | t0127 | g0007 | EAS | CDX | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02165 | hp2 | a0001 | c0001 | t0008 | g0176 | EAS | CDX | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02257 | hp1 | a0002 | c0002 | t0166 | g0018 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02257 | hp2 | a0001 | c0003 | t0039 | g0179 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02258 | hp1 | a0001 | c0001 | t0049 | g0020 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02258 | hp2 | a0001 | c0001 | t0036 | g0094 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02273 | hp1 | a0001 | c0001 | t0009 | g0085 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02273 | hp2 | a0001 | c0001 | t0121 | g0016 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02280 | hp1 | a0001 | c0001 | t0079 | g0151 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02280 | hp2 | a0001 | c0001 | t0053 | g0019 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02300 | hp1 | a0001 | c0001 | t0068 | g0013 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02300 | hp2 | a0001 | c0001 | t0120 | g0016 | AMR | PEL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02451 | hp1 | a0001 | c0001 | t0024 | g0109 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02451 | hp2 | a0001 | c0001 | t0150 | g0095 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02523 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02523 | hp2 | a0001 | c0001 | t0023 | g0150 | EAS | KHV | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02572 | hp1 | a0001 | c0001 | t0034 | g0035 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02572 | hp2 | a0001 | c0001 | t0106 | g0081 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02602 | hp1 | a0001 | c0001 | t0017 | g0002 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0101 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02615 | hp1 | a0001 | c0001 | t0014 | g0189 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02615 | hp2 | a0001 | c0001 | t0015 | g0119 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02622 | hp1 | a0001 | c0001 | t0044 | g0124 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02622 | hp2 | a0001 | c0001 | t0179 | g0019 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02630 | hp1 | a0001 | c0001 | t0168 | g0019 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02630 | hp2 | a0001 | c0001 | t0104 | g0020 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02647 | hp1 | a0001 | c0001 | t0039 | g0025 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02647 | hp2 | a0001 | c0001 | t0053 | g0019 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02683 | hp1 | a0001 | c0001 | t0136 | g0042 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02683 | hp2 | a0001 | c0001 | t0011 | g0037 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02698 | hp1 | a0001 | c0001 | t0170 | g0131 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02698 | hp2 | a0001 | c0001 | t0148 | g0075 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02717 | hp1 | a0001 | c0001 | t0021 | g0056 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02717 | hp2 | a0001 | c0001 | t0015 | g0152 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02723 | hp1 | a0001 | c0001 | t0173 | g0196 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02723 | hp2 | a0001 | c0001 | t0081 | g0118 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02735 | hp1 | a0001 | c0001 | t0008 | g0001 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02735 | hp2 | a0001 | c0001 | t0069 | g0121 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02738 | hp1 | a0001 | c0001 | t0162 | g0157 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02738 | hp2 | a0001 | c0001 | t0094 | g0004 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02818 | hp1 | a0001 | c0001 | t0034 | g0034 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02818 | hp2 | a0001 | c0001 | t0147 | g0108 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02886 | hp1 | a0001 | c0001 | t0141 | g0017 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02886 | hp2 | a0001 | c0001 | t0151 | g0033 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02895 | hp1 | a0001 | c0001 | t0163 | g0021 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02895 | hp2 | a0001 | c0001 | t0164 | g0021 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02896 | hp1 | a0001 | c0003 | t0116 | g0047 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02896 | hp2 | a0002 | c0002 | t0172 | g0183 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02897 | hp1 | a0001 | c0003 | t0071 | g0047 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02897 | hp2 | a0001 | c0001 | t0052 | g0009 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02922 | hp1 | a0001 | c0001 | t0152 | g0035 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02965 | hp1 | a0001 | c0001 | t0024 | g0107 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02965 | hp2 | a0001 | c0001 | t0193 | g0027 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02970 | hp1 | a0001 | c0001 | t0038 | g0191 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02970 | hp2 | a0001 | c0001 | t0084 | g0117 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02976 | hp1 | a0001 | c0001 | t0178 | g0190 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03017 | hp1 | a0001 | c0001 | t0114 | g0100 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03017 | hp2 | a0001 | c0001 | t0020 | g0002 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0052 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03041 | hp2 | a0001 | c0001 | t0038 | g0097 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03098 | hp1 | a0001 | c0001 | t0128 | g0103 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03098 | hp2 | a0001 | c0001 | t0014 | g0014 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03130 | hp1 | a0001 | c0001 | t0126 | g0104 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03130 | hp2 | a0001 | c0001 | t0034 | g0034 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03139 | hp1 | a0001 | c0001 | t0085 | g0148 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03139 | hp2 | a0001 | c0001 | t0021 | g0031 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03195 | hp1 | a0002 | c0002 | t0175 | g0048 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03195 | hp2 | a0001 | c0001 | t0087 | g0033 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03209 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03209 | hp2 | a0001 | c0001 | t0167 | g0127 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03225 | hp1 | a0001 | c0001 | t0052 | g0009 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03225 | hp2 | a0001 | c0001 | t0195 | g0014 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03239 | hp1 | a0001 | c0001 | t0009 | g0086 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03239 | hp2 | a0001 | c0001 | t0009 | g0002 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03453 | hp2 | a0001 | c0001 | t0024 | g0105 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03486 | hp1 | a0001 | c0001 | t0107 | g0076 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03486 | hp2 | a0003 | c0006 | t0082 | g0159 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03490 | hp1 | a0001 | c0001 | t0018 | g0005 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03490 | hp2 | a0001 | c0001 | t0022 | g0036 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03491 | hp1 | a0001 | c0001 | t0043 | g0012 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03491 | hp2 | a0001 | c0001 | t0074 | g0002 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03492 | hp1 | a0001 | c0001 | t0043 | g0045 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03492 | hp2 | a0001 | c0001 | t0022 | g0036 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03516 | hp1 | a0001 | c0001 | t0161 | g0125 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03516 | hp2 | a0001 | c0001 | t0020 | g0060 | AFR | ESN | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03540 | hp1 | a0001 | c0001 | t0075 | g0106 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03540 | hp2 | a0001 | c0001 | t0015 | g0003 | AFR | GWD | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03579 | hp1 | a0001 | c0001 | t0197 | g0014 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03579 | hp2 | a0001 | c0001 | t0110 | g0001 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03654 | hp1 | a0001 | c0001 | t0011 | g0099 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03654 | hp2 | a0001 | c0001 | t0131 | g0002 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03669 | hp1 | a0001 | c0001 | t0064 | g0017 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03669 | hp2 | a0001 | c0001 | t0186 | g0010 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03688 | hp1 | a0001 | c0001 | t0115 | g0001 | SAS | STU | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03688 | hp2 | a0001 | c0001 | t0042 | g0006 | SAS | STU | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03704 | hp1 | a0001 | c0001 | t0017 | g0002 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03704 | hp2 | a0001 | c0001 | t0135 | g0002 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03710 | hp1 | a0001 | c0001 | t0028 | g0061 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03710 | hp2 | a0001 | c0001 | t0060 | g0037 | SAS | PJL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03831 | hp1 | a0001 | c0001 | t0123 | g0074 | SAS | BEB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03831 | hp2 | a0001 | c0001 | t0194 | g0194 | SAS | BEB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03834 | hp1 | a0001 | c0001 | t0048 | g0083 | SAS | BEB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03834 | hp2 | a0001 | c0001 | t0025 | g0137 | SAS | BEB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03927 | hp2 | a0001 | c0001 | t0185 | g0042 | SAS | BEB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | BEB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03942 | hp2 | a0001 | c0001 | t0017 | g0087 | SAS | BEB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG04115 | hp1 | a0001 | c0001 | t0124 | g0013 | SAS | STU | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG04115 | hp2 | a0001 | c0001 | t0196 | g0005 | SAS | STU | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0132 | SAS | BEB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG04184 | hp2 | a0001 | c0001 | t0042 | g0067 | SAS | BEB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG04204 | hp1 | a0001 | c0001 | t0028 | g0059 | SAS | STU | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG04204 | hp2 | a0001 | c0001 | t0057 | g0142 | SAS | STU | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG04228 | hp1 | a0001 | c0001 | t0032 | g0001 | SAS | STU | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG04228 | hp2 | a0001 | c0001 | t0113 | g0038 | SAS | STU | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18522 | hp1 | a0002 | c0002 | t0169 | g0018 | AFR | YRI | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18522 | hp2 | a0001 | c0001 | t0149 | g0093 | AFR | YRI | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18612 | hp1 | a0001 | c0001 | t0018 | g0005 | EAS | CHB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18612 | hp2 | a0001 | c0001 | t0183 | g0001 | EAS | CHB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18747 | hp1 | a0001 | c0001 | t0096 | g0001 | EAS | CHB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18747 | hp2 | a0001 | c0001 | t0032 | g0167 | EAS | CHB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18939 | hp1 | a0001 | c0001 | t0154 | g0088 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18939 | hp2 | a0001 | c0001 | t0207 | g0003 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18942 | hp1 | a0001 | c0001 | t0204 | g0003 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18942 | hp2 | a0001 | c0001 | t0023 | g0003 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18943 | hp1 | a0001 | c0001 | t0083 | g0141 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18945 | hp1 | a0001 | c0001 | t0095 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18945 | hp2 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18948 | hp1 | a0001 | c0001 | t0142 | g0003 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18949 | hp1 | a0001 | c0001 | t0007 | g0177 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18949 | hp2 | a0001 | c0001 | t0025 | g0010 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18951 | hp1 | a0001 | c0001 | t0035 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18951 | hp2 | a0001 | c0001 | t0122 | g0002 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18959 | hp1 | a0001 | c0001 | t0018 | g0049 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18959 | hp2 | a0001 | c0001 | t0035 | g0178 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18962 | hp2 | a0001 | c0001 | t0073 | g0024 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18967 | hp1 | a0001 | c0001 | t0019 | g0091 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18968 | hp1 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18968 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18969 | hp1 | a0001 | c0001 | t0092 | g0039 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18969 | hp2 | a0001 | c0001 | t0047 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18970 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18971 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18971 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18974 | hp2 | a0001 | c0001 | t0030 | g0156 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18977 | hp2 | a0001 | c0001 | t0059 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18979 | hp1 | a0001 | c0001 | t0117 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18979 | hp2 | a0001 | c0001 | t0016 | g0024 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18981 | hp1 | a0001 | c0001 | t0037 | g0171 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18983 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18983 | hp2 | a0001 | c0001 | t0033 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18984 | hp1 | a0001 | c0001 | t0198 | g0005 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18985 | hp1 | a0001 | c0001 | t0145 | g0163 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18987 | hp1 | a0001 | c0001 | t0019 | g0025 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18987 | hp2 | a0001 | c0001 | t0066 | g0007 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18990 | hp1 | a0001 | c0001 | t0006 | g0166 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18991 | hp1 | a0001 | c0001 | t0190 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18991 | hp2 | a0001 | c0001 | t0205 | g0120 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18993 | hp1 | a0001 | c0001 | t0139 | g0170 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18993 | hp2 | a0001 | c0001 | t0061 | g0007 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18994 | hp1 | a0001 | c0001 | t0016 | g0023 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18994 | hp2 | a0001 | c0001 | t0067 | g0007 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18995 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18995 | hp2 | a0001 | c0001 | t0201 | g0187 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18998 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18999 | hp1 | a0001 | c0001 | t0018 | g0049 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19000 | hp2 | a0001 | c0001 | t0016 | g0041 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19001 | hp2 | a0001 | c0001 | t0044 | g0115 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19009 | hp1 | a0001 | c0001 | t0029 | g0025 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19009 | hp2 | a0001 | c0001 | t0046 | g0082 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19010 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19010 | hp2 | a0001 | c0001 | t0153 | g0041 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19011 | hp1 | a0001 | c0001 | t0137 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19011 | hp2 | a0001 | c0001 | t0129 | g0102 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19012 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19012 | hp2 | a0001 | c0001 | t0077 | g0003 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19030 | hp1 | a0001 | c0001 | t0027 | g0065 | AFR | LWK | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19030 | hp2 | a0001 | c0001 | t0014 | g0188 | AFR | LWK | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19043 | hp1 | a0001 | c0001 | t0056 | g0027 | AFR | LWK | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19043 | hp2 | a0004 | c0004 | t0048 | g0002 | AFR | LWK | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19054 | hp1 | a0001 | c0001 | t0029 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19054 | hp2 | a0001 | c0001 | t0030 | g0161 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19057 | hp1 | a0001 | c0001 | t0133 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19057 | hp2 | a0001 | c0001 | t0026 | g0043 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19058 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19058 | hp2 | a0001 | c0001 | t0208 | g0054 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19062 | hp1 | a0001 | c0001 | t0188 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19062 | hp2 | a0001 | c0001 | t0027 | g0129 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19063 | hp1 | a0001 | c0001 | t0184 | g0089 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19063 | hp2 | a0001 | c0001 | t0033 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19065 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19066 | hp1 | a0001 | c0001 | t0051 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19067 | hp1 | a0001 | c0001 | t0025 | g0039 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19067 | hp2 | a0001 | c0001 | t0134 | g0055 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19070 | hp1 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19070 | hp2 | a0001 | c0001 | t0033 | g0046 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19072 | hp1 | a0001 | c0001 | t0065 | g0057 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19072 | hp2 | a0001 | c0001 | t0072 | g0173 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19074 | hp2 | a0001 | c0001 | t0031 | g0002 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19075 | hp1 | a0001 | c0001 | t0023 | g0053 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19075 | hp2 | a0001 | c0001 | t0019 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19076 | hp2 | a0005 | c0005 | t0029 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19077 | hp1 | a0001 | c0001 | t0037 | g0044 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19077 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19078 | hp1 | a0001 | c0001 | t0055 | g0192 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19078 | hp2 | a0001 | c0001 | t0032 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19081 | hp2 | a0001 | c0001 | t0062 | g0180 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19082 | hp1 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19082 | hp2 | a0001 | c0001 | t0007 | g0175 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19088 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19090 | hp1 | a0001 | c0001 | t0155 | g0123 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19090 | hp2 | a0001 | c0001 | t0040 | g0001 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19091 | hp1 | a0001 | c0001 | t0018 | g0028 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19091 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19240 | hp1 | a0001 | c0001 | t0036 | g0009 | AFR | YRI | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA19240 | hp2 | a0002 | c0002 | t0177 | g0018 | AFR | YRI | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ASW | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA20129 | hp2 | a0001 | c0001 | t0174 | g0195 | AFR | ASW | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA20752 | hp1 | a0001 | c0001 | t0020 | g0020 | EUR | TSI | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA20752 | hp2 | a0001 | c0001 | t0020 | g0072 | EUR | TSI | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA20805 | hp1 | a0001 | c0001 | t0010 | g0005 | EUR | TSI | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA20905 | hp1 | a0001 | c0001 | t0098 | g0162 | SAS | GIH | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA20905 | hp2 | a0001 | c0001 | t0105 | g0002 | SAS | GIH | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01123 | hp1 | a0001 | c0001 | t0010 | g0005 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0069 | AMR | CLM | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02109 | hp1 | a0001 | c0001 | t0076 | g0158 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02109 | hp2 | a0001 | c0001 | t0015 | g0140 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02486 | hp2 | a0001 | c0001 | t0202 | g0030 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02559 | hp1 | a0001 | c0001 | t0021 | g0030 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG02559 | hp2 | a0001 | c0001 | t0014 | g0186 | AFR | ACB | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG03471 | hp2 | a0001 | c0001 | t0118 | g0181 | AFR | MSL | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG06807 | hp1 | a0001 | c0001 | t0203 | g0005 | AFR | USA | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
HG06807 | hp2 | a0001 | c0001 | t0080 | g0147 | AFR | USA | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA18955 | hp2 | a0001 | c0001 | t0108 | g0044 | EAS | JPT | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA20300 | hp1 | a0001 | c0001 | t0056 | g0027 | AFR | USA | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA20300 | hp2 | a0002 | c0002 | t0165 | g0018 | AFR | USA | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA21309 | hp1 | a0001 | c0001 | t0200 | g0005 | AFR | LWK | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
NA21309 | hp2 | a0001 | c0001 | t0078 | g0096 | AFR | LWK | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
homoSapiens | chm13v2 | a0001 | c0001 | t0130 | g0078 | REF | REF | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0029 | REF | REF | TRIM13_chr13_49992042_50023467 | TRIM13 | chr13 | 49992042 | 50023467 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:50012398 | G | A | 1 | a0004 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.458G>A | p.Arg153His | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1186/7255 | 458/1224 | 153/407 | chr13 | 50012398 | |||
chr13:50012760 | G | A | 1 | a0005 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.820G>A | p.Ala274Thr | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1548/7255 | 820/1224 | 274/407 | chr13 | 50012760 | |||
chr13:50012844 | G | A | 1 | a0003 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.904G>A | p.Asp302Asn | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1632/7255 | 904/1224 | 302/407 | chr13 | 50012844 | |||
chr13:50013004 | G | C | 1 | a0002 | 11 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(8): Show |
missense_variant | MODERATE | c.1064G>C | p.Ser355Thr | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1792/7255 | 1064/1224 | 355/407 | chr13 | 50013004 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:50013068 | A | G | 1 | a0001c0003 | 3 | HG02257.hp2 HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.1128A>G | p.Thr376Thr | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1856/7255 | 1128/1224 | 376/407 | chr13 | 50013068 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:49997074 | C | T | 5 | a0001c0001t0204 a0001c0001t0205 a0001c0001t0206 others(2): Show |
5 | HG00423.hp1 NA18939.hp2 NA18942.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-696C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/2 | chr13 | 49997074 | |||||||
chr13:49997165 | C | G | 18 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(15): Show |
37 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(34): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-605C>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/2 | chr13 | 49997165 | |||||||
chr13:49997173 | C | CG | 7 | a0001c0001t0057 a0001c0001t0058 a0001c0001t0059 others(4): Show |
7 | HG02056.hp1 HG02145.hp1 HG03710.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-593dupG | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/2 | 14763 | INFO_REALIGN_3_PRIME | chr13 | 49997173 | |||||
chr13:49997239 | T | TG | 10 | a0001c0001t0055 a0001c0001t0184 a0001c0001t0185 others(7): Show |
11 | HG00741.hp2 HG01192.hp1 HG02071.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-524dupG | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/2 | 14694 | INFO_REALIGN_3_PRIME | chr13 | 49997239 | |||||
chr13:49997336 | G | A | 1 | a0001c0001t0064 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-434G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/2 | 14605 | chr13 | 49997336 | ||||||
chr13:49997485 | G | C | 1 | a0001c0001t0065 | 1 | NA19072.hp1 | 5_prime_UTR_variant | MODIFIER | c.-285G>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/2 | 14456 | chr13 | 49997485 | ||||||
chr13:49997505 | C | T | 1 | a0001c0001t0183 | 1 | NA18612.hp2 | 5_prime_UTR_variant | MODIFIER | c.-265C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/2 | 14436 | chr13 | 49997505 | ||||||
chr13:49997573 | T | G | 2 | a0001c0001t0066 a0001c0001t0067 |
2 | NA18987.hp2 NA18994.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-197T>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/2 | chr13 | 49997573 | |||||||
chr13:50013262 | C | G | 2 | a0001c0001t0036 a0001c0001t0182 |
4 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*98C>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 98 | chr13 | 50013262 | ||||||
chr13:50013275 | C | T | 2 | a0001c0001t0180 a0001c0001t0181 |
2 | HG00733.hp2 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*111C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 111 | chr13 | 50013275 | ||||||
chr13:50013501 | G | T | 2 | a0001c0001t0036 a0001c0001t0182 |
4 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*337G>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 337 | chr13 | 50013501 | ||||||
chr13:50013518 | C | CT | 28 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(25): Show |
49 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*376dupT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 377 | INFO_REALIGN_3_PRIME | chr13 | 50013518 | |||||
chr13:50013518 | CT | C | 118 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(115): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*376delT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 376 | INFO_REALIGN_3_PRIME | chr13 | 50013518 | |||||
chr13:50013518 | CTT | C | 31 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0022 others(28): Show |
51 | HG00323.hp2 HG00408.hp2 HG01433.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*375_*376delTT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 375 | INFO_REALIGN_3_PRIME | chr13 | 50013518 | |||||
chr13:50013582 | A | G | 201 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(198): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*418A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 418 | chr13 | 50013582 | ||||||
chr13:50013587 | A | G | 1 | a0001c0001t0148 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*423A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 423 | chr13 | 50013587 | ||||||
chr13:50014313 | CA | C | 12 | a0001c0001t0021 a0001c0001t0048 a0001c0001t0131 others(9): Show |
15 | HG00735.hp2 HG01106.hp2 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1181delA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1181 | INFO_REALIGN_3_PRIME | chr13 | 50014313 | |||||
chr13:50014313 | CAA | C | 9 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0049 others(6): Show |
22 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1180_*1181delAA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1180 | INFO_REALIGN_3_PRIME | chr13 | 50014313 | |||||
chr13:50014313 | CAAA | C | 8 | a0001c0001t0020 a0001c0001t0135 a0001c0001t0144 others(5): Show |
11 | HG01192.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1179_*1181delAAA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1179 | INFO_REALIGN_3_PRIME | chr13 | 50014313 | |||||
chr13:50014313 | CAAAA | C | 10 | a0001c0001t0014 a0001c0001t0018 a0001c0001t0056 others(7): Show |
20 | HG01192.hp2 HG01496.hp1 HG01993.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1181delAAAA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1178 | INFO_REALIGN_3_PRIME | chr13 | 50014313 | |||||
chr13:50014313 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0179 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1172_*1181delAAAA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1172 | INFO_REALIGN_3_PRIME | chr13 | 50014313 | |||||
chr13:50014327 | A | C | 1 | a0001c0001t0152 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1163A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1163 | chr13 | 50014327 | ||||||
chr13:50014334 | A | ATATATAT others(8): Show |
1 | a0002c0002t0177 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1170_*1171insTATA others(11): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1171 | chr13 | 50014334 | ||||||
chr13:50014334 | A | T | 4 | a0001c0001t0021 a0001c0001t0146 a0001c0001t0178 others(1): Show |
8 | HG00323.hp1 HG01106.hp2 HG01167.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1170A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1170 | chr13 | 50014334 | ||||||
chr13:50014336 | A | ATATATAT others(8): Show |
1 | a0002c0002t0169 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1172_*1173insTATA others(11): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1173 | chr13 | 50014336 | ||||||
chr13:50014336 | A | T | 8 | a0001c0001t0021 a0001c0001t0146 a0001c0001t0147 others(5): Show |
12 | HG00323.hp1 HG01106.hp2 HG01167.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1172A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1172 | chr13 | 50014336 | ||||||
chr13:50014338 | A | AT | 4 | a0001c0001t0015 a0001c0001t0023 a0001c0001t0085 others(1): Show |
10 | HG01891.hp1 HG02109.hp2 HG02523.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1174_*1175insT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1175 | chr13 | 50014338 | ||||||
chr13:50014338 | A | T | 24 | a0001c0001t0010 a0001c0001t0021 a0001c0001t0053 others(21): Show |
36 | HG00323.hp1 HG00733.hp1 HG00738.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1174A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1174 | chr13 | 50014338 | ||||||
chr13:50014340 | A | AT | 3 | a0001c0001t0076 a0002c0002t0165 a0002c0002t0171 |
3 | HG01109.hp2 HG02109.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1176_*1177insT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1177 | chr13 | 50014340 | ||||||
chr13:50014340 | A | ATAT | 4 | a0001c0001t0038 a0001c0001t0057 a0001c0001t0077 others(1): Show |
5 | HG02896.hp2 HG02970.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1176_*1177insTAT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1177 | chr13 | 50014340 | ||||||
chr13:50014340 | A | ATATAT | 3 | a0001c0001t0078 a0001c0001t0079 a0001c0001t0080 |
3 | HG02280.hp1 HG06807.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1176_*1177insTATA others(1): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1177 | chr13 | 50014340 | ||||||
chr13:50014340 | A | T | 54 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0014 others(51): Show |
93 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1176A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1176 | chr13 | 50014340 | ||||||
chr13:50014342 | A | ATATAT | 4 | a0001c0001t0050 a0001c0001t0133 a0001c0001t0134 others(1): Show |
5 | HG00741.hp2 HG01175.hp2 HG02148.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179insTATA others(1): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1179 | chr13 | 50014342 | ||||||
chr13:50014342 | A | ATATATAT | 4 | a0001c0001t0012 a0001c0001t0033 a0001c0001t0051 others(1): Show |
12 | HG00099.hp2 HG02027.hp2 NA18968.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179insTATA others(3): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1179 | chr13 | 50014342 | ||||||
chr13:50014342 | A | T | 79 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0014 others(76): Show |
122 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1178A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1178 | chr13 | 50014342 | ||||||
chr13:50014344 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0152 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAA others(16): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0026 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAA others(9): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0002 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAA others(11): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0026 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAA others(7): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0091 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAA others(10): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0002 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAA others(11): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0002 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAA others(8): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAAAAAT others(8): Show |
1 | a0001c0001t0025 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAA others(11): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAAAATA others(7): Show |
1 | a0001c0001t0002 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAA others(10): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAAATAT others(4): Show |
1 | a0001c0001t0025 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAT others(7): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAAATAT others(6): Show |
1 | a0001c0001t0092 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAAAT others(9): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAATATA others(3): Show |
3 | a0001c0001t0006 a0001c0001t0041 a0001c0001t0157 |
3 | HG00558.hp1 HG01169.hp2 HG02027.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAATA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAATATA others(5): Show |
1 | a0001c0001t0041 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAATA others(8): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAAATATA others(7): Show |
1 | a0001c0001t0024 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insAATA others(10): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAATATAT | 10 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0027 others(7): Show |
16 | HG00597.hp2 HG01243.hp1 HG01433.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1181_*1182insATAT others(3): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAATATAT others(2): Show |
5 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0025 others(2): Show |
8 | HG02647.hp1 NA18941.hp2 NA18949.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1181_*1182insATAT others(5): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | AAATATAT others(6): Show |
1 | a0001c0001t0024 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181_*1182insATAT others(9): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | INFO_REALIGN_3_PRIME | chr13 | 50014344 | |||||
chr13:50014344 | A | ATAT | 5 | a0001c0001t0001 a0001c0001t0031 a0001c0001t0068 others(2): Show |
5 | HG01358.hp2 HG02300.hp1 HG02735.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1180_*1181insTAT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1181 | chr13 | 50014344 | ||||||
chr13:50014344 | A | ATATAT | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0040 others(5): Show |
11 | HG00408.hp1 HG00738.hp2 HG01081.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1180_*1181insTATA others(1): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1181 | chr13 | 50014344 | ||||||
chr13:50014344 | A | ATATATAT | 12 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(9): Show |
25 | HG00140.hp2 HG00544.hp2 HG00673.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1180_*1181insTATA others(3): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1181 | chr13 | 50014344 | ||||||
chr13:50014344 | A | ATATATAT others(2): Show |
2 | a0001c0001t0006 a0001c0001t0040 |
3 | NA18945.hp2 NA18990.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1180_*1181insTATA others(5): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1181 | chr13 | 50014344 | ||||||
chr13:50014344 | A | ATATATAT others(6): Show |
1 | a0001c0001t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1180_*1181insTATA others(9): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1181 | chr13 | 50014344 | ||||||
chr13:50014344 | A | T | 128 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(125): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*1180A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1180 | chr13 | 50014344 | ||||||
chr13:50014346 | T | A | 6 | a0001c0001t0019 a0001c0001t0032 a0001c0001t0061 others(3): Show |
7 | HG00621.hp1 HG02074.hp1 HG04228.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1182T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1182 | chr13 | 50014346 | ||||||
chr13:50014358 | T | C | 2 | a0001c0001t0146 a0001c0001t0167 |
2 | HG00323.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1194T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1194 | chr13 | 50014358 | ||||||
chr13:50014360 | T | C | 35 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0021 others(32): Show |
58 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1196T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1196 | chr13 | 50014360 | ||||||
chr13:50014360 | T | TAC | 11 | a0001c0001t0003 a0001c0001t0064 a0001c0001t0065 others(8): Show |
21 | HG00408.hp2 HG00423.hp1 HG01433.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1212_*1213dupCA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1214 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TACAC | 15 | a0001c0001t0002 a0001c0001t0038 a0001c0001t0066 others(12): Show |
29 | HG00408.hp1 HG00673.hp1 HG01975.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1210_*1213dupCACA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1214 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TACACAC | 5 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0068 others(2): Show |
8 | HG00544.hp1 HG01081.hp2 HG01256.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1208_*1213dupCACA others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1214 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TACACACA others(1): Show |
14 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(11): Show |
42 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1206_*1213dupCACA others(4): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1214 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TACACACA others(3): Show |
3 | a0001c0001t0050 a0001c0001t0093 a0001c0001t0133 |
4 | HG01175.hp2 HG01981.hp1 HG02148.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1204_*1213dupCACA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1214 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATAC | 2 | a0001c0001t0022 a0001c0001t0143 |
4 | HG00639.hp1 HG02083.hp1 HG03490.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTACA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATACACA others(3): Show |
1 | a0001c0001t0108 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTACA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATACA others(1): Show |
8 | a0001c0001t0011 a0001c0001t0044 a0001c0001t0060 others(5): Show |
14 | HG00621.hp2 HG00741.hp1 HG01109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(4): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATACA others(3): Show |
3 | a0001c0001t0030 a0001c0001t0112 a0001c0001t0159 |
5 | HG00423.hp2 HG02074.hp1 HG02135.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATACA others(5): Show |
4 | a0001c0001t0029 a0001c0001t0110 a0001c0001t0111 others(1): Show |
5 | HG00597.hp1 HG03579.hp2 NA19009.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(8): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATACA others(7): Show |
3 | a0001c0001t0043 a0001c0001t0109 a0001c0001t0137 |
4 | HG01167.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(10): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(1): Show |
5 | a0001c0001t0016 a0001c0001t0045 a0001c0001t0073 others(2): Show |
10 | HG00558.hp2 HG01255.hp1 HG01981.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(4): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(3): Show |
6 | a0001c0001t0005 a0001c0001t0061 a0001c0001t0067 others(3): Show |
15 | HG00609.hp2 HG02738.hp1 HG03516.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(5): Show |
2 | a0001c0001t0072 a0001c0001t0118 |
2 | HG03471.hp2 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(8): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(7): Show |
5 | a0001c0001t0008 a0001c0001t0062 a0001c0001t0117 others(2): Show |
11 | HG01074.hp2 HG01099.hp1 HG01358.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(10): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(11): Show |
1 | a0001c0001t0115 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(14): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(3): Show |
3 | a0001c0001t0075 a0001c0001t0126 a0001c0001t0127 |
3 | HG02165.hp1 HG03130.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(5): Show |
1 | a0001c0001t0125 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(8): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(9): Show |
7 | a0001c0001t0019 a0001c0001t0035 a0001c0001t0037 others(4): Show |
14 | HG00609.hp1 HG01496.hp2 HG01517.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(12): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(5): Show |
1 | a0001c0001t0128 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(8): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(11): Show |
1 | a0001c0001t0032 | 3 | HG04228.hp1 NA18747.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(14): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(7): Show |
1 | a0002c0002t0054 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(10): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(9): Show |
1 | a0001c0001t0129 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(12): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(13): Show |
1 | a0001c0001t0139 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(16): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(15): Show |
1 | a0001c0001t0140 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(18): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(17): Show |
1 | a0002c0002t0166 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(20): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014360 | T | TATATATA others(15): Show |
3 | a0002c0002t0063 a0002c0002t0165 a0002c0002t0171 |
3 | HG01109.hp2 HG02145.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insTATA others(18): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | INFO_REALIGN_3_PRIME | chr13 | 50014360 | |||||
chr13:50014362 | C | T | 18 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0020 others(15): Show |
35 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1198C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1198 | chr13 | 50014362 | ||||||
chr13:50014364 | C | T | 19 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0020 others(16): Show |
36 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1200C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1200 | chr13 | 50014364 | ||||||
chr13:50014366 | C | T | 19 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0020 others(16): Show |
36 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1202C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1202 | chr13 | 50014366 | ||||||
chr13:50014478 | T | G | 1 | a0001c0001t0098 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314T>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1314 | chr13 | 50014478 | ||||||
chr13:50014646 | A | G | 1 | a0001c0001t0162 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1482A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1482 | chr13 | 50014646 | ||||||
chr13:50014687 | CAA | C | 5 | a0001c0001t0053 a0001c0001t0168 a0001c0001t0173 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1525_*1526delAA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1525 | INFO_REALIGN_3_PRIME | chr13 | 50014687 | |||||
chr13:50014892 | T | G | 1 | a0001c0001t0099 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1728T>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1728 | chr13 | 50014892 | ||||||
chr13:50015075 | TA | T | 8 | a0001c0001t0057 a0001c0001t0067 a0001c0001t0085 others(5): Show |
8 | HG00639.hp1 HG02015.hp2 HG02027.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1931delA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015075 | |||||
chr13:50015075 | TAAA | T | 8 | a0001c0001t0044 a0001c0001t0066 a0001c0001t0073 others(5): Show |
9 | HG00609.hp2 HG02015.hp1 HG02080.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1929_*1931delAAA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1929 | INFO_REALIGN_3_PRIME | chr13 | 50015075 | |||||
chr13:50015075 | TAAAAA | T | 6 | a0001c0001t0092 a0001c0001t0097 a0001c0001t0112 others(3): Show |
7 | HG00423.hp2 HG00544.hp1 HG01167.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1927_*1931delAAAA others(1): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015075 | |||||
chr13:50015081 | AAAAAAAA others(28): Show |
A | 1 | a0001c0001t0200 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1919_*1953delAAAA others(31): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1919 | INFO_REALIGN_3_PRIME | chr13 | 50015081 | |||||
chr13:50015082 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0010 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1920_*1947delAAAA others(24): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1920 | INFO_REALIGN_3_PRIME | chr13 | 50015082 | |||||
chr13:50015083 | AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0018 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1921_*1939delAAAA others(15): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1921 | INFO_REALIGN_3_PRIME | chr13 | 50015083 | |||||
chr13:50015083 | AAAAAAAA others(28): Show |
A | 1 | a0001c0001t0196 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1921_*1955delAAAA others(31): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1921 | INFO_REALIGN_3_PRIME | chr13 | 50015083 | |||||
chr13:50015084 | AAAAAAAA others(27): Show |
A | 2 | a0001c0001t0010 a0001c0001t0193 |
2 | HG01123.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1922_*1955delAAAA others(30): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1922 | INFO_REALIGN_3_PRIME | chr13 | 50015084 | |||||
chr13:50015085 | AAAAAAAA others(20): Show |
A | 2 | a0001c0001t0002 a0001c0001t0005 |
2 | HG04184.hp1 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1923_*1949delAAAA others(23): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1923 | INFO_REALIGN_3_PRIME | chr13 | 50015085 | |||||
chr13:50015085 | AAAAAAAA others(22): Show |
A | 2 | a0001c0001t0018 a0001c0001t0201 |
2 | NA18612.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1923_*1951delAAAA others(25): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1923 | INFO_REALIGN_3_PRIME | chr13 | 50015085 | |||||
chr13:50015085 | AAAAAAAA others(24): Show |
A | 1 | a0001c0001t0198 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1923_*1953delAAAA others(27): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1923 | INFO_REALIGN_3_PRIME | chr13 | 50015085 | |||||
chr13:50015085 | AAAAAAAA others(40): Show |
A | 1 | a0001c0001t0018 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1923_*1969delAAAA others(43): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1923 | INFO_REALIGN_3_PRIME | chr13 | 50015085 | |||||
chr13:50015086 | A | T | 1 | a0001c0001t0002 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1922A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1922 | chr13 | 50015086 | ||||||
chr13:50015086 | AAAAAAAA others(27): Show |
A | 4 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0056 others(1): Show |
6 | HG00738.hp1 HG01099.hp2 HG01192.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1924_*1957delAAAA others(30): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1924 | INFO_REALIGN_3_PRIME | chr13 | 50015086 | |||||
chr13:50015086 | AAAAAAAA others(33): Show |
A | 1 | a0001c0001t0194 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1924_*1963delAAAA others(36): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1924 | INFO_REALIGN_3_PRIME | chr13 | 50015086 | |||||
chr13:50015087 | AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0003 a0001c0001t0016 |
2 | NA19000.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1925_*1935delAAAA others(7): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1925 | INFO_REALIGN_3_PRIME | chr13 | 50015087 | |||||
chr13:50015087 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0023 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1925_*1937delAAAA others(9): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1925 | INFO_REALIGN_3_PRIME | chr13 | 50015087 | |||||
chr13:50015087 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0002 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1925_*1947delAAAA others(19): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1925 | INFO_REALIGN_3_PRIME | chr13 | 50015087 | |||||
chr13:50015087 | AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0005 | 2 | NA18966.hp1 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1925_*1949delAAAA others(21): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1925 | INFO_REALIGN_3_PRIME | chr13 | 50015087 | |||||
chr13:50015087 | AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0014 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1925_*1951delAAAA others(23): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1925 | INFO_REALIGN_3_PRIME | chr13 | 50015087 | |||||
chr13:50015087 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0027 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1925_*1953delAAAA others(25): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1925 | INFO_REALIGN_3_PRIME | chr13 | 50015087 | |||||
chr13:50015087 | AAAAAAAA others(26): Show |
A | 4 | a0001c0001t0010 a0001c0001t0191 a0001c0001t0199 others(1): Show |
4 | HG01106.hp1 HG01496.hp1 HG01993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1925_*1957delAAAA others(29): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1925 | INFO_REALIGN_3_PRIME | chr13 | 50015087 | |||||
chr13:50015087 | AAAAAAAA others(40): Show |
A | 1 | a0001c0001t0005 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1925_*1971delAAAA others(43): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1925 | INFO_REALIGN_3_PRIME | chr13 | 50015087 | |||||
chr13:50015088 | A | T | 2 | a0001c0001t0002 a0001c0001t0195 |
2 | HG01975.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1924A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1924 | chr13 | 50015088 | ||||||
chr13:50015088 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0006 a0001c0001t0016 |
2 | HG00558.hp1 HG00558.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1926_*1935delAAAA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1926 | INFO_REALIGN_3_PRIME | chr13 | 50015088 | |||||
chr13:50015088 | AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0014 a0001c0001t0136 a0001c0001t0197 |
3 | HG02683.hp1 HG03471.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1926_*1937delAAAA others(8): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1926 | INFO_REALIGN_3_PRIME | chr13 | 50015088 | |||||
chr13:50015088 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0030 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1926_*1939delAAAA others(10): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1926 | INFO_REALIGN_3_PRIME | chr13 | 50015088 | |||||
chr13:50015088 | AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0159 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1926_*1949delAAAA others(20): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1926 | INFO_REALIGN_3_PRIME | chr13 | 50015088 | |||||
chr13:50015088 | AAAAAAAA others(27): Show |
A | 1 | a0001c0001t0010 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1926_*1959delAAAA others(30): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1926 | INFO_REALIGN_3_PRIME | chr13 | 50015088 | |||||
chr13:50015089 | AAAAAAAT others(4): Show |
A | 4 | a0001c0001t0006 a0001c0001t0027 a0001c0001t0055 others(1): Show |
4 | HG01516.hp2 HG02071.hp1 NA18939.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1927_*1937delAAAA others(7): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(6): Show |
A | 1 | a0001c0001t0055 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1939delAAAA others(9): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0030 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1941delAAAA others(11): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(10): Show |
A | 1 | a0001c0001t0006 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1943delAAAA others(13): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(14): Show |
A | 1 | a0001c0001t0144 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1947delAAAA others(17): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(18): Show |
A | 2 | a0001c0001t0002 a0001c0001t0030 |
2 | NA18943.hp2 NA18974.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1927_*1951delAAAA others(21): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(20): Show |
A | 2 | a0001c0001t0026 a0001c0001t0127 |
2 | HG02165.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1927_*1953delAAAA others(23): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(22): Show |
A | 2 | a0001c0001t0002 a0001c0001t0018 |
3 | NA18999.hp1 NA19076.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1927_*1955delAAAA others(25): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(24): Show |
A | 2 | a0001c0001t0005 a0001c0001t0006 |
2 | HG02155.hp1 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1927_*1957delAAAA others(27): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(28): Show |
A | 1 | a0001c0001t0064 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1961delAAAA others(31): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(32): Show |
A | 1 | a0001c0001t0002 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1965delAAAA others(35): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(34): Show |
A | 1 | a0001c0001t0006 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1967delAAAA others(37): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(38): Show |
A | 1 | a0001c0001t0026 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1971delAAAA others(41): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015089 | AAAAAAAT others(40): Show |
A | 1 | a0001c0001t0005 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1973delAAAA others(43): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | INFO_REALIGN_3_PRIME | chr13 | 50015089 | |||||
chr13:50015090 | A | AATATATA others(5): Show |
1 | a0001c0001t0163 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1928insTATA others(8): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1928 | INFO_REALIGN_3_PRIME | chr13 | 50015090 | |||||
chr13:50015090 | A | AT | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(2): Show |
5 | HG00423.hp1 HG02004.hp1 NA18942.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1926_*1927insT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1927 | chr13 | 50015090 | ||||||
chr13:50015090 | A | T | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(4): Show |
8 | HG01975.hp1 HG02148.hp2 HG03017.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1926A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1926 | chr13 | 50015090 | ||||||
chr13:50015090 | AAAAAATA others(3): Show |
A | 1 | a0002c0002t0165 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1928_*1937delAAAA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1928 | INFO_REALIGN_3_PRIME | chr13 | 50015090 | |||||
chr13:50015090 | AAAAAATA others(5): Show |
A | 1 | a0001c0001t0006 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1928_*1939delAAAA others(8): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1928 | INFO_REALIGN_3_PRIME | chr13 | 50015090 | |||||
chr13:50015090 | AAAAAATA others(7): Show |
A | 1 | a0001c0001t0002 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1928_*1941delAAAA others(10): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1928 | INFO_REALIGN_3_PRIME | chr13 | 50015090 | |||||
chr13:50015090 | AAAAAATA others(11): Show |
A | 1 | a0001c0001t0021 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1928_*1945delAAAA others(14): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1928 | INFO_REALIGN_3_PRIME | chr13 | 50015090 | |||||
chr13:50015090 | AAAAAATA others(17): Show |
A | 1 | a0001c0001t0174 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1928_*1951delAAAA others(20): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1928 | INFO_REALIGN_3_PRIME | chr13 | 50015090 | |||||
chr13:50015090 | AAAAAATA others(25): Show |
A | 1 | a0002c0002t0172 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1928_*1959delAAAA others(28): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1928 | INFO_REALIGN_3_PRIME | chr13 | 50015090 | |||||
chr13:50015090 | AAAAAATA others(27): Show |
A | 1 | a0001c0001t0010 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1928_*1961delAAAA others(30): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1928 | INFO_REALIGN_3_PRIME | chr13 | 50015090 | |||||
chr13:50015090 | AAAAAATA others(35): Show |
A | 3 | a0001c0001t0038 a0001c0001t0078 a0001c0001t0141 |
3 | HG02886.hp1 HG03041.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1928_*1969delAAAA others(38): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1928 | INFO_REALIGN_3_PRIME | chr13 | 50015090 | |||||
chr13:50015091 | AAAAATAT others(4): Show |
A | 2 | a0001c0001t0170 a0001c0001t0205 |
2 | HG02698.hp1 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1929_*1939delAAAT others(7): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1929 | INFO_REALIGN_3_PRIME | chr13 | 50015091 | |||||
chr13:50015091 | AAAAATAT others(10): Show |
A | 1 | a0001c0001t0098 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1929_*1945delAAAT others(13): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1929 | INFO_REALIGN_3_PRIME | chr13 | 50015091 | |||||
chr13:50015091 | AAAAATAT others(16): Show |
A | 3 | a0001c0001t0015 a0001c0001t0145 a0001c0001t0162 |
3 | HG02109.hp2 HG02738.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1929_*1951delAAAT others(19): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1929 | INFO_REALIGN_3_PRIME | chr13 | 50015091 | |||||
chr13:50015091 | AAAAATAT others(18): Show |
A | 1 | a0001c0001t0090 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1929_*1953delAAAT others(21): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1929 | INFO_REALIGN_3_PRIME | chr13 | 50015091 | |||||
chr13:50015091 | AAAAATAT others(20): Show |
A | 2 | a0001c0001t0077 a0001c0001t0089 |
2 | HG00099.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1929_*1955delAAAT others(23): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1929 | INFO_REALIGN_3_PRIME | chr13 | 50015091 | |||||
chr13:50015091 | AAAAATAT others(24): Show |
A | 1 | a0001c0001t0041 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1929_*1959delAAAT others(27): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1929 | INFO_REALIGN_3_PRIME | chr13 | 50015091 | |||||
chr13:50015091 | AAAAATAT others(26): Show |
A | 1 | a0001c0001t0011 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1929_*1961delAAAT others(29): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1929 | INFO_REALIGN_3_PRIME | chr13 | 50015091 | |||||
chr13:50015091 | AAAAATAT others(34): Show |
A | 2 | a0001c0001t0038 a0001c0001t0080 |
2 | HG02970.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1929_*1969delAAAT others(37): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1929 | INFO_REALIGN_3_PRIME | chr13 | 50015091 | |||||
chr13:50015092 | A | T | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(17): Show |
24 | HG00423.hp1 HG00621.hp1 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1928A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1928 | chr13 | 50015092 | ||||||
chr13:50015092 | AAAATATA others(3): Show |
A | 2 | a0001c0001t0003 a0001c0001t0075 |
2 | HG03540.hp1 NA18974.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1930_*1939delAATA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1930 | INFO_REALIGN_3_PRIME | chr13 | 50015092 | |||||
chr13:50015092 | AAAATATA others(11): Show |
A | 1 | a0001c0001t0021 | 2 | HG01106.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1930_*1947delAATA others(14): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1930 | INFO_REALIGN_3_PRIME | chr13 | 50015092 | |||||
chr13:50015092 | AAAATATA others(15): Show |
A | 4 | a0001c0001t0027 a0001c0001t0053 a0001c0001t0168 others(1): Show |
5 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1930_*1951delAATA others(18): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1930 | INFO_REALIGN_3_PRIME | chr13 | 50015092 | |||||
chr13:50015092 | AAAATATA others(17): Show |
A | 2 | a0001c0001t0046 a0001c0001t0156 |
2 | HG00735.hp1 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1930_*1953delAATA others(20): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1930 | INFO_REALIGN_3_PRIME | chr13 | 50015092 | |||||
chr13:50015092 | AAAATATA others(19): Show |
A | 10 | a0001c0001t0004 a0001c0001t0031 a0001c0001t0042 others(7): Show |
20 | HG00323.hp2 HG01123.hp2 HG01175.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1930_*1955delAATA others(22): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1930 | INFO_REALIGN_3_PRIME | chr13 | 50015092 | |||||
chr13:50015092 | AAAATATA others(21): Show |
A | 10 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0020 others(7): Show |
14 | HG00733.hp2 HG01081.hp1 HG01978.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1930_*1957delAATA others(24): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1930 | INFO_REALIGN_3_PRIME | chr13 | 50015092 | |||||
chr13:50015092 | AAAATATA others(23): Show |
A | 2 | a0001c0001t0041 a0001c0001t0106 |
2 | HG01169.hp2 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1930_*1959delAATA others(26): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1930 | INFO_REALIGN_3_PRIME | chr13 | 50015092 | |||||
chr13:50015092 | AAAATATA others(35): Show |
A | 3 | a0001c0001t0079 a0001c0001t0081 a0001c0001t0084 |
3 | HG02280.hp1 HG02723.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1930_*1971delAATA others(38): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1930 | INFO_REALIGN_3_PRIME | chr13 | 50015092 | |||||
chr13:50015093 | A | AT | 3 | a0001c0001t0035 a0001c0001t0068 a0001c0001t0146 |
3 | HG00323.hp1 HG02300.hp1 NA18951.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1929_*1930insT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1930 | chr13 | 50015093 | ||||||
chr13:50015093 | A | T | 2 | a0001c0001t0035 a0001c0001t0095 |
2 | HG02074.hp2 NA18945.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1929A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1929 | chr13 | 50015093 | ||||||
chr13:50015093 | AAAT | A | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(6): Show |
10 | HG00639.hp2 HG01167.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1931_*1933delATA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATAT | A | 10 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(7): Show |
10 | HG01175.hp2 HG02135.hp1 HG03579.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1931_*1935delATAT others(1): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT | A | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(6): Show |
14 | HG00673.hp2 HG00741.hp2 HG01099.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1931_*1937delATAT others(3): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(2): Show |
A | 9 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(6): Show |
15 | HG00099.hp2 HG00738.hp2 HG01168.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1931_*1939delATAT others(5): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(4): Show |
A | 5 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0093 others(2): Show |
6 | HG01074.hp2 HG01981.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1931_*1941delATAT others(7): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(6): Show |
A | 4 | a0001c0001t0012 a0001c0001t0032 a0001c0001t0043 others(1): Show |
5 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1931_*1943delATAT others(9): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(8): Show |
A | 2 | a0001c0001t0040 a0001c0003t0039 |
2 | HG01081.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1931_*1945delATAT others(11): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(10): Show |
A | 2 | a0001c0001t0131 a0001c0001t0149 |
2 | HG03654.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1931_*1947delATAT others(13): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(12): Show |
A | 1 | a0001c0001t0118 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1931_*1949delATAT others(15): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(14): Show |
A | 2 | a0001c0001t0003 a0001c0001t0202 |
2 | HG00408.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1931_*1951delATAT others(17): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(16): Show |
A | 2 | a0001c0001t0046 a0001c0001t0135 |
2 | HG03704.hp2 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1931_*1953delATAT others(19): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(18): Show |
A | 3 | a0001c0001t0031 a0001c0001t0049 a0001c0001t0132 |
4 | HG00140.hp1 HG00735.hp2 HG01358.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1931_*1955delATAT others(21): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(20): Show |
A | 6 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0020 others(3): Show |
14 | HG01192.hp1 HG01361.hp2 HG01934.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1931_*1957delATAT others(23): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(24): Show |
A | 2 | a0001c0001t0122 a0001c0001t0190 |
2 | NA18951.hp2 NA18991.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1931_*1961delATAT others(27): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(26): Show |
A | 10 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0033 others(7): Show |
22 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1931_*1963delATAT others(29): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(28): Show |
A | 2 | a0001c0001t0103 a0001c0001t0124 |
2 | HG00140.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1931_*1965delATAT others(31): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015093 | AAATATAT others(34): Show |
A | 1 | a0001c0001t0011 | 2 | HG00741.hp1 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1931_*1971delATAT others(37): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | INFO_REALIGN_3_PRIME | chr13 | 50015093 | |||||
chr13:50015094 | A | AAATATAT others(10): Show |
1 | a0001c0001t0052 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1931_*1932insATAT others(13): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1932 | INFO_REALIGN_3_PRIME | chr13 | 50015094 | |||||
chr13:50015094 | A | AATATATA others(9): Show |
1 | a0001c0001t0164 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1972_*1987dupTATA others(12): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1988 | INFO_REALIGN_3_PRIME | chr13 | 50015094 | |||||
chr13:50015094 | A | T | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(38): Show |
52 | HG00323.hp1 HG00423.hp1 HG00609.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1930A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1930 | chr13 | 50015094 | ||||||
chr13:50015094 | AATATATA others(3): Show |
A | 1 | a0001c0001t0024 | 2 | HG02451.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1978_*1987delTATA others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1978 | INFO_REALIGN_3_PRIME | chr13 | 50015094 | |||||
chr13:50015094 | AATATATA others(5): Show |
A | 1 | a0001c0001t0126 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1976_*1987delTATA others(8): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1976 | INFO_REALIGN_3_PRIME | chr13 | 50015094 | |||||
chr13:50015094 | AATATATA others(7): Show |
A | 1 | a0001c0001t0087 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1974_*1987delTATA others(10): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1974 | INFO_REALIGN_3_PRIME | chr13 | 50015094 | |||||
chr13:50015094 | AATATATA others(9): Show |
A | 1 | a0001c0001t0151 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1972_*1987delTATA others(12): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1972 | INFO_REALIGN_3_PRIME | chr13 | 50015094 | |||||
chr13:50015094 | AATATATA others(17): Show |
A | 1 | a0001c0001t0150 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964_*1987delTATA others(20): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1964 | INFO_REALIGN_3_PRIME | chr13 | 50015094 | |||||
chr13:50015094 | AATATATA others(31): Show |
A | 3 | a0001c0001t0013 a0001c0001t0036 a0001c0001t0182 |
6 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1950_*1987delTATA others(34): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1950 | INFO_REALIGN_3_PRIME | chr13 | 50015094 | |||||
chr13:50015094 | AATATATA others(33): Show |
A | 1 | a0001c0001t0178 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1948_*1987delTATA others(36): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1948 | INFO_REALIGN_3_PRIME | chr13 | 50015094 | |||||
chr13:50015095 | A | T | 2 | a0001c0001t0040 a0001c0001t0108 |
2 | NA18955.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1931A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1931 | chr13 | 50015095 | ||||||
chr13:50015095 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0128 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1932_*1942delTATA others(7): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1932 | chr13 | 50015095 | ||||||
chr13:50015095 | ATATATAT others(34): Show |
A | 3 | a0001c0001t0060 a0001c0001t0069 a0001c0001t0113 |
3 | HG02735.hp2 HG03710.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1932_*1972delTATA others(37): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1932 | chr13 | 50015095 | ||||||
chr13:50015097 | A | T | 9 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(6): Show |
10 | HG00639.hp2 HG01167.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1933A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1933 | chr13 | 50015097 | ||||||
chr13:50015099 | A | T | 10 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(7): Show |
10 | HG01175.hp2 HG02135.hp1 HG03579.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1935A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1935 | chr13 | 50015099 | ||||||
chr13:50015100 | T | A | 1 | a0001c0001t0161 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1936T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1936 | chr13 | 50015100 | ||||||
chr13:50015101 | A | T | 8 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0050 others(5): Show |
13 | HG00673.hp2 HG00741.hp2 HG01099.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1937A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1937 | chr13 | 50015101 | ||||||
chr13:50015102 | T | A | 1 | a0001c0001t0024 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1938T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1938 | chr13 | 50015102 | ||||||
chr13:50015103 | A | T | 9 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(6): Show |
15 | HG00099.hp2 HG00738.hp2 HG01168.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1939A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1939 | chr13 | 50015103 | ||||||
chr13:50015104 | T | A | 1 | a0001c0001t0147 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1940T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1940 | chr13 | 50015104 | ||||||
chr13:50015105 | A | T | 5 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0093 others(2): Show |
6 | HG01074.hp2 HG01981.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1941A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1941 | chr13 | 50015105 | ||||||
chr13:50015106 | T | A | 1 | a0001c0001t0024 | 2 | HG02451.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1942T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1942 | chr13 | 50015106 | ||||||
chr13:50015107 | A | T | 4 | a0001c0001t0012 a0001c0001t0032 a0001c0001t0043 others(1): Show |
5 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1943A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1943 | chr13 | 50015107 | ||||||
chr13:50015108 | T | A | 1 | a0001c0001t0126 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1944T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1944 | chr13 | 50015108 | ||||||
chr13:50015109 | A | T | 2 | a0001c0001t0040 a0001c0003t0039 |
2 | HG01081.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1945A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1945 | chr13 | 50015109 | ||||||
chr13:50015110 | T | A | 1 | a0001c0001t0126 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1946T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1946 | chr13 | 50015110 | ||||||
chr13:50015111 | A | T | 1 | a0001c0001t0131 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1947A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1947 | chr13 | 50015111 | ||||||
chr13:50015113 | A | T | 1 | a0001c0001t0118 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1949A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1949 | chr13 | 50015113 | ||||||
chr13:50015115 | A | T | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1951A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1951 | chr13 | 50015115 | ||||||
chr13:50015117 | A | T | 4 | a0001c0001t0046 a0001c0001t0090 a0001c0001t0135 others(1): Show |
5 | HG00735.hp1 HG01069.hp1 HG01256.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1953A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1953 | chr13 | 50015117 | ||||||
chr13:50015119 | A | T | 12 | a0001c0001t0004 a0001c0001t0031 a0001c0001t0042 others(9): Show |
25 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1955A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1955 | chr13 | 50015119 | ||||||
chr13:50015121 | A | T | 13 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0020 others(10): Show |
29 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1957A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1957 | chr13 | 50015121 | ||||||
chr13:50015123 | A | T | 2 | a0001c0001t0041 a0001c0001t0106 |
3 | HG01168.hp2 HG01169.hp2 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1959A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1959 | chr13 | 50015123 | ||||||
chr13:50015125 | A | T | 2 | a0001c0001t0122 a0001c0001t0190 |
2 | NA18951.hp2 NA18991.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1961A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1961 | chr13 | 50015125 | ||||||
chr13:50015127 | A | T | 10 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0033 others(7): Show |
22 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1963A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1963 | chr13 | 50015127 | ||||||
chr13:50015129 | A | T | 2 | a0001c0001t0103 a0001c0001t0124 |
2 | HG00140.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1965A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1965 | chr13 | 50015129 | ||||||
chr13:50015136 | T | A | 1 | a0001c0001t0178 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1972T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1972 | chr13 | 50015136 | ||||||
chr13:50015138 | T | A | 1 | a0001c0001t0178 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1974T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1974 | chr13 | 50015138 | ||||||
chr13:50015140 | T | A | 1 | a0001c0001t0178 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1976T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1976 | chr13 | 50015140 | ||||||
chr13:50015142 | T | A | 1 | a0001c0001t0178 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1978T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 1978 | chr13 | 50015142 | ||||||
chr13:50015430 | T | A | 1 | a0001c0001t0094 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2266T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 2266 | chr13 | 50015430 | ||||||
chr13:50016124 | C | A | 5 | a0001c0001t0024 a0001c0001t0075 a0001c0001t0126 others(2): Show |
7 | HG02451.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2960C>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 2960 | chr13 | 50016124 | ||||||
chr13:50016156 | T | TCTC | 34 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(31): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2994_*2995insCCT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 2995 | INFO_REALIGN_3_PRIME | chr13 | 50016156 | |||||
chr13:50016206 | T | C | 2 | a0001c0001t0100 a0001c0001t0125 |
2 | HG00621.hp1 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3042T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 3042 | chr13 | 50016206 | ||||||
chr13:50016287 | G | C | 43 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(40): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*3123G>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 3123 | chr13 | 50016287 | ||||||
chr13:50016567 | C | T | 1 | a0001c0001t0104 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3403C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 3403 | chr13 | 50016567 | ||||||
chr13:50016702 | C | G | 34 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(31): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3538C>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 3538 | chr13 | 50016702 | ||||||
chr13:50016734 | C | T | 1 | a0001c0001t0123 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3570C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 3570 | chr13 | 50016734 | ||||||
chr13:50016735 | A | C | 18 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0023 others(15): Show |
32 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3571A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 3571 | chr13 | 50016735 | ||||||
chr13:50016863 | CT | C | 188 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(185): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
3_prime_UTR_variant | MODIFIER | c.*3715delT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 3715 | INFO_REALIGN_3_PRIME | chr13 | 50016863 | |||||
chr13:50016887 | G | T | 1 | a0001c0001t0087 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3723G>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 3723 | chr13 | 50016887 | ||||||
chr13:50017206 | T | A | 34 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(31): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*4042T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 4042 | chr13 | 50017206 | ||||||
chr13:50017480 | A | G | 10 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0033 others(7): Show |
22 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4316A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 4316 | chr13 | 50017480 | ||||||
chr13:50017481 | C | T | 1 | a0001c0001t0110 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4317C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 4317 | chr13 | 50017481 | ||||||
chr13:50017637 | T | C | 2 | a0001c0001t0198 a0001c0001t0201 |
2 | NA18984.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4473T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 4473 | chr13 | 50017637 | ||||||
chr13:50017718 | T | C | 6 | a0001c0001t0018 a0001c0001t0194 a0001c0001t0196 others(3): Show |
10 | HG03490.hp1 HG03831.hp2 HG04115.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4554T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 4554 | chr13 | 50017718 | ||||||
chr13:50017924 | T | G | 18 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(15): Show |
37 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4760T>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 4760 | chr13 | 50017924 | ||||||
chr13:50017994 | A | G | 1 | a0001c0001t0109 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4830A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 4830 | chr13 | 50017994 | ||||||
chr13:50018169 | C | T | 1 | a0001c0001t0080 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5005C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 5005 | chr13 | 50018169 | ||||||
chr13:50018318 | T | A | 1 | a0001c0001t0095 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5154T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 5154 | chr13 | 50018318 | ||||||
chr13:50018321 | T | C | 1 | a0001c0001t0095 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5157T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 5157 | chr13 | 50018321 | ||||||
chr13:50018322 | T | A | 1 | a0001c0001t0095 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5158T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 5158 | chr13 | 50018322 | ||||||
chr13:50018323 | T | C | 10 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0055 others(7): Show |
23 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5159T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 5159 | chr13 | 50018323 | ||||||
chr13:50018324 | A | G | 1 | a0001c0001t0095 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5160A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 5160 | chr13 | 50018324 | ||||||
chr13:50018327 | A | T | 1 | a0001c0001t0095 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5163A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 5163 | chr13 | 50018327 | ||||||
chr13:50018331 | G | A | 1 | a0001c0001t0095 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5167G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 5167 | chr13 | 50018331 | ||||||
chr13:50018390 | C | T | 1 | a0001c0001t0096 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5226C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 5226 | chr13 | 50018390 | ||||||
chr13:50018436 | T | G | 18 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(15): Show |
37 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*5272T>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 2/2 | 5272 | chr13 | 50018436 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:49997792 | C | CT | 309 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(306): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.-7+39dupT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 49997792 | ||||||
chr13:49997792 | C | CTT | 8 | a0001c0001t0053g0019 a0001c0001t0055g0192 a0001c0001t0168g0019 others(5): Show |
9 | HG02145.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+38_-7+39dupTT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 49997792 | ||||||
chr13:49997911 | T | C | 1 | a0001c0001t0065g0057 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-7+148T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49997911 | |||||||
chr13:49998304 | G | A | 1 | a0001c0001t0137g0001 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-7+541G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49998304 | |||||||
chr13:49998314 | G | T | 1 | a0001c0001t0038g0191 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7+551G>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49998314 | |||||||
chr13:49998552 | G | C | 53 | a0001c0001t0004g0006 a0001c0001t0004g0032 a0001c0001t0004g0062 others(50): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.-7+789G>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49998552 | |||||||
chr13:49998884 | C | T | 1 | a0002c0002t0054g0050 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-7+1121C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49998884 | |||||||
chr13:49998914 | A | G | 3 | a0001c0001t0053g0019 a0001c0001t0168g0019 a0001c0001t0179g0019 |
4 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+1151A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49998914 | |||||||
chr13:49998914 | A | T | 1 | a0001c0001t0178g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-7+1151A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49998914 | |||||||
chr13:49998917 | G | T | 5 | a0001c0001t0053g0019 a0001c0001t0168g0019 a0001c0001t0173g0196 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+1154G>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49998917 | |||||||
chr13:49998927 | C | CA | 8 | a0001c0001t0001g0090 a0001c0001t0019g0091 a0001c0001t0028g0059 others(5): Show |
8 | HG01069.hp1 HG04204.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+1179dupA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 49998927 | ||||||
chr13:49998927 | CAA | C | 41 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(38): Show |
54 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.-7+1178_-7+1179del others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 49998927 | ||||||
chr13:49998944 | C | G | 1 | a0001c0001t0001g0182 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-7+1181C>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49998944 | |||||||
chr13:49999079 | ACTCCCTT others(32): Show |
A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(127): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.-7+1350_-7+1388del others(39): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 49999079 | ||||||
chr13:49999292 | C | T | 4 | a0001c0001t0006g0165 a0001c0001t0006g0166 a0001c0001t0016g0164 others(1): Show |
4 | HG02080.hp2 NA18945.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+1529C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49999292 | |||||||
chr13:49999314 | A | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(306): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-7+1551A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49999314 | |||||||
chr13:49999393 | G | A | 2 | a0001c0001t0038g0097 a0001c0001t0078g0096 |
2 | HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-7+1630G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49999393 | |||||||
chr13:49999440 | T | C | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-7+1677T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49999440 | |||||||
chr13:49999504 | A | G | 1 | a0001c0001t0021g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-7+1741A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49999504 | |||||||
chr13:49999546 | T | C | 2 | a0001c0001t0087g0033 a0001c0001t0151g0033 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-7+1783T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49999546 | |||||||
chr13:49999783 | T | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(73): Show |
95 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-7+2020T>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49999783 | |||||||
chr13:49999827 | A | G | 1 | a0001c0001t0017g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-7+2064A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49999827 | |||||||
chr13:49999850 | T | C | 5 | a0001c0001t0053g0019 a0001c0001t0168g0019 a0001c0001t0173g0196 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+2087T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 49999850 | |||||||
chr13:50000063 | C | A | 19 | a0001c0001t0011g0099 a0001c0001t0027g0098 a0001c0001t0053g0019 others(16): Show |
21 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7+2300C>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000063 | |||||||
chr13:50000183 | T | C | 1 | a0001c0001t0032g0167 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-7+2420T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000183 | |||||||
chr13:50000270 | T | A | 1 | a0001c0001t0020g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-7+2507T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000270 | |||||||
chr13:50000294 | C | A | 1 | a0001c0001t0003g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-7+2531C>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000294 | |||||||
chr13:50000379 | T | C | 1 | a0001c0001t0129g0102 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-7+2616T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000379 | |||||||
chr13:50000389 | A | C | 1 | a0001c0001t0062g0180 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-7+2626A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000389 | |||||||
chr13:50000415 | T | C | 4 | a0001c0001t0014g0186 a0001c0001t0056g0027 a0001c0001t0192g0185 others(1): Show |
5 | HG01192.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+2652T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000415 | |||||||
chr13:50000424 | A | G | 1 | a0001c0001t0009g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-7+2661A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000424 | |||||||
chr13:50000502 | C | T | 3 | a0001c0003t0039g0179 a0001c0003t0071g0047 a0001c0003t0116g0047 |
3 | HG02257.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-7+2739C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000502 | |||||||
chr13:50000565 | C | A | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-7+2802C>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000565 | |||||||
chr13:50000620 | A | T | 1 | a0001c0001t0098g0162 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-7+2857A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000620 | |||||||
chr13:50000695 | AGTG | A | 5 | a0001c0001t0053g0019 a0001c0001t0168g0019 a0001c0001t0173g0196 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+2936_-7+2938del others(3): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50000695 | ||||||
chr13:50000733 | TTCTC | T | 22 | a0001c0001t0004g0006 a0001c0001t0004g0032 a0001c0001t0004g0062 others(19): Show |
25 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-7+2974_-7+2977del others(4): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50000733 | ||||||
chr13:50000758 | T | C | 1 | a0002c0002t0172g0183 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-7+2995T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50000758 | |||||||
chr13:50000770 | A | ATT | 129 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0010 others(126): Show |
146 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.-7+3010_-7+3011dup others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50000770 | ||||||
chr13:50000934 | GAGC | G | 16 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0022 others(13): Show |
22 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7+3174_-7+3176del others(3): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50000934 | ||||||
chr13:50001080 | A | G | 2 | a0001c0001t0030g0160 a0001c0001t0030g0161 |
2 | HG02135.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-7+3317A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50001080 | |||||||
chr13:50001171 | A | G | 2 | a0001c0001t0076g0158 a0003c0006t0082g0159 |
2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-7+3408A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50001171 | |||||||
chr13:50001264 | C | A | 5 | a0001c0001t0053g0019 a0001c0001t0168g0019 a0001c0001t0173g0196 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+3501C>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50001264 | |||||||
chr13:50001291 | C | CA | 23 | a0001c0001t0001g0090 a0001c0001t0001g0169 a0001c0001t0003g0116 others(20): Show |
25 | HG00609.hp2 HG00673.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.-7+3546dupA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50001291 | ||||||
chr13:50001291 | C | CAA | 48 | a0001c0001t0004g0006 a0001c0001t0004g0032 a0001c0001t0004g0062 others(45): Show |
57 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-7+3545_-7+3546dup others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50001291 | ||||||
chr13:50001335 | A | G | 1 | a0001c0001t0144g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-7+3572A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50001335 | |||||||
chr13:50001480 | A | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(306): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-7+3717A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50001480 | |||||||
chr13:50001717 | A | G | 1 | a0001c0001t0162g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-7+3954A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50001717 | |||||||
chr13:50001751 | A | G | 1 | a0001c0001t0150g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-7+3988A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50001751 | |||||||
chr13:50001818 | T | C | 1 | a0001c0001t0205g0120 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-7+4055T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50001818 | |||||||
chr13:50002209 | C | T | 1 | a0001c0001t0046g0082 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-7+4446C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50002209 | |||||||
chr13:50002252 | G | A | 10 | a0002c0002t0054g0050 a0002c0002t0063g0193 a0002c0002t0165g0018 others(7): Show |
11 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7+4489G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50002252 | |||||||
chr13:50002380 | CTG | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(127): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.-7+4619_-7+4620del others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50002380 | ||||||
chr13:50002388 | AAAAAAC | A | 6 | a0001c0001t0026g0043 a0001c0001t0030g0156 a0001c0001t0030g0160 others(3): Show |
6 | HG00423.hp2 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+4641_-7+4646del others(6): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50002388 | ||||||
chr13:50002411 | C | T | 5 | a0001c0001t0053g0019 a0001c0001t0168g0019 a0001c0001t0173g0196 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+4648C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50002411 | |||||||
chr13:50002421 | C | T | 2 | a0001c0001t0157g0153 a0001c0001t0158g0154 |
2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.-7+4658C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50002421 | |||||||
chr13:50002489 | T | C | 1 | a0001c0001t0020g0072 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-7+4726T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50002489 | |||||||
chr13:50002660 | C | T | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-7+4897C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50002660 | |||||||
chr13:50002751 | C | T | 43 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0101 others(40): Show |
48 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-7+4988C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50002751 | |||||||
chr13:50002761 | C | T | 1 | a0001c0003t0039g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7+4998C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50002761 | |||||||
chr13:50002824 | G | A | 6 | a0002c0002t0063g0193 a0002c0002t0165g0018 a0002c0002t0166g0018 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+5061G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50002824 | |||||||
chr13:50002916 | C | G | 1 | a0001c0001t0091g0139 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-7+5153C>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50002916 | |||||||
chr13:50003051 | C | T | 53 | a0001c0001t0004g0006 a0001c0001t0004g0032 a0001c0001t0004g0062 others(50): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.-7+5288C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50003051 | |||||||
chr13:50003314 | C | T | 1 | a0001c0001t0178g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-7+5551C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50003314 | |||||||
chr13:50003368 | C | A | 5 | a0001c0001t0053g0019 a0001c0001t0168g0019 a0001c0001t0173g0196 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+5605C>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50003368 | |||||||
chr13:50003430 | C | T | 1 | a0001c0001t0006g0166 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-7+5667C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50003430 | |||||||
chr13:50003732 | C | G | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-7+5969C>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50003732 | |||||||
chr13:50003886 | T | C | 4 | a0001c0001t0021g0030 a0001c0001t0021g0031 a0001c0001t0021g0056 others(1): Show |
5 | HG01106.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+6123T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50003886 | |||||||
chr13:50003899 | G | A | 1 | a0001c0001t0069g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-7+6136G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50003899 | |||||||
chr13:50003899 | G | T | 1 | a0001c0001t0004g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-7+6136G>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50003899 | |||||||
chr13:50003906 | G | A | 1 | a0001c0001t0015g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7+6143G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50003906 | |||||||
chr13:50004053 | G | A | 5 | a0001c0001t0053g0019 a0001c0001t0168g0019 a0001c0001t0173g0196 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+6290G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50004053 | |||||||
chr13:50004233 | C | T | 1 | a0001c0001t0015g0152 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-7+6470C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50004233 | |||||||
chr13:50004358 | T | C | 1 | a0001c0001t0139g0170 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-7+6595T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50004358 | |||||||
chr13:50004441 | G | A | 26 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(23): Show |
37 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-7+6678G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50004441 | |||||||
chr13:50004667 | C | T | 2 | a0001c0001t0002g0138 a0001c0001t0044g0115 |
2 | NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-7+6904C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50004667 | |||||||
chr13:50004808 | G | A | 1 | a0001c0001t0189g0073 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-7+7045G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50004808 | |||||||
chr13:50004907 | CTCTACTA others(2698): Show |
C | 3 | a0001c0003t0039g0179 a0001c0003t0071g0047 a0001c0003t0116g0047 |
3 | HG02257.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-6-7003_-6-4299del | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50004907 | ||||||
chr13:50005444 | C | T | 1 | a0001c0001t0044g0124 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-6-6491C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50005444 | |||||||
chr13:50005607 | G | A | 1 | a0001c0001t0015g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-6-6328G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50005607 | |||||||
chr13:50005686 | G | A | 2 | a0001c0001t0066g0007 a0001c0001t0067g0007 |
2 | NA18987.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-6-6249G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50005686 | |||||||
chr13:50005740 | G | GT | 24 | a0001c0001t0002g0130 a0001c0001t0002g0133 a0001c0001t0005g0022 others(21): Show |
24 | HG00423.hp1 HG00741.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.-6-6179dupT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50005740 | ||||||
chr13:50005792 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0182 a0001c0001t0004g0064 others(6): Show |
10 | HG01516.hp1 HG01517.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.-6-6143C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50005792 | |||||||
chr13:50005840 | C | T | 1 | a0001c0001t0013g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-6-6095C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50005840 | |||||||
chr13:50005919 | G | A | 1 | a0001c0001t0159g0155 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-6-6016G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50005919 | |||||||
chr13:50005944 | C | T | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-6-5991C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50005944 | |||||||
chr13:50005953 | C | T | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-6-5982C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50005953 | |||||||
chr13:50005994 | C | T | 1 | a0001c0001t0200g0005 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-6-5941C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50005994 | |||||||
chr13:50006066 | A | C | 1 | a0001c0001t0162g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-6-5869A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50006066 | |||||||
chr13:50006136 | T | TAAA | 41 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(38): Show |
54 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.-6-5799_-6-5798ins others(3): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50006136 | |||||||
chr13:50006137 | G | A | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-6-5798G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50006137 | |||||||
chr13:50006621 | G | A | 1 | a0001c0001t0163g0021 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-6-5314G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50006621 | |||||||
chr13:50006776 | C | T | 9 | a0002c0002t0054g0050 a0002c0002t0063g0193 a0002c0002t0165g0018 others(6): Show |
10 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-6-5159C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50006776 | |||||||
chr13:50006792 | T | G | 2 | a0001c0001t0031g0002 a0001c0001t0049g0020 |
2 | HG01975.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-6-5143T>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50006792 | |||||||
chr13:50007107 | C | T | 2 | a0001c0001t0098g0162 a0001c0001t0186g0010 |
2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-6-4828C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007107 | |||||||
chr13:50007108 | G | A | 1 | a0001c0001t0058g0011 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-6-4827G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007108 | |||||||
chr13:50007165 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(71): Show |
93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.-6-4770G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007165 | |||||||
chr13:50007182 | C | CA | 6 | a0001c0001t0026g0043 a0001c0001t0055g0192 a0001c0001t0072g0173 others(3): Show |
6 | HG01069.hp1 HG02074.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-4740dupA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50007182 | ||||||
chr13:50007182 | CA | C | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-6-4740delA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50007182 | ||||||
chr13:50007195 | A | C | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-6-4740A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007195 | |||||||
chr13:50007267 | G | A | 1 | a0001c0001t0032g0001 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-6-4668G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007267 | |||||||
chr13:50007360 | C | T | 2 | a0001c0001t0180g0066 a0001c0001t0181g0006 |
2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-6-4575C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007360 | |||||||
chr13:50007401 | G | T | 1 | a0001c0001t0185g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-6-4534G>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007401 | |||||||
chr13:50007440 | G | A | 1 | a0001c0001t0027g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-6-4495G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007440 | |||||||
chr13:50007470 | A | G | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-6-4465A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007470 | |||||||
chr13:50007488 | C | CA | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0002g0022 others(54): Show |
59 | HG00423.hp2 HG00609.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6-4431dupA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50007488 | ||||||
chr13:50007535 | C | T | 4 | a0001c0001t0021g0030 a0001c0001t0021g0031 a0001c0001t0021g0056 others(1): Show |
5 | HG01106.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-4400C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007535 | |||||||
chr13:50007656 | C | T | 67 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0010 others(64): Show |
77 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-6-4279C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007656 | |||||||
chr13:50007659 | TA | T | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-6-4273delA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50007659 | ||||||
chr13:50007706 | C | G | 1 | a0001c0001t0025g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-6-4229C>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007706 | |||||||
chr13:50007717 | G | A | 1 | a0001c0001t0038g0191 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-6-4218G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007717 | |||||||
chr13:50007782 | C | CA | 12 | a0001c0001t0002g0130 a0001c0001t0003g0143 a0001c0001t0014g0188 others(9): Show |
13 | HG00544.hp1 HG01361.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-4137dupA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50007782 | ||||||
chr13:50007782 | C | CAA | 5 | a0001c0001t0053g0019 a0001c0001t0168g0019 a0001c0001t0173g0196 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-4138_-6-4137dup others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50007782 | ||||||
chr13:50007782 | C | CAAA | 12 | a0001c0001t0021g0030 a0001c0001t0021g0031 a0001c0001t0021g0056 others(9): Show |
14 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-4139_-6-4137dup others(3): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50007782 | ||||||
chr13:50007782 | C | CAAAAA | 18 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(15): Show |
27 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-6-4141_-6-4137dup others(5): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50007782 | ||||||
chr13:50007782 | CA | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(126): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.-6-4137delA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50007782 | ||||||
chr13:50007785 | A | C | 2 | a0001c0001t0037g0171 a0001c0001t0123g0074 |
2 | HG03831.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-6-4150A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007785 | |||||||
chr13:50007786 | A | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(125): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-6-4149A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007786 | |||||||
chr13:50007908 | C | T | 19 | a0001c0001t0006g0011 a0001c0001t0006g0023 a0001c0001t0006g0024 others(16): Show |
22 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.-6-4027C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50007908 | |||||||
chr13:50008223 | C | T | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-6-3712C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50008223 | |||||||
chr13:50008359 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-6-3576G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50008359 | |||||||
chr13:50008429 | G | A | 1 | a0001c0001t0004g0071 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-6-3506G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50008429 | |||||||
chr13:50008452 | G | A | 7 | a0001c0001t0024g0105 a0001c0001t0024g0107 a0001c0001t0024g0109 others(4): Show |
7 | HG02451.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-3483G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50008452 | |||||||
chr13:50008478 | CA | C | 27 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(24): Show |
38 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.-6-3447delA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50008478 | ||||||
chr13:50008527 | A | C | 4 | a0001c0001t0021g0030 a0001c0001t0021g0031 a0001c0001t0021g0056 others(1): Show |
5 | HG01106.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-3408A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50008527 | |||||||
chr13:50008605 | T | G | 3 | a0001c0003t0039g0179 a0001c0003t0071g0047 a0001c0003t0116g0047 |
3 | HG02257.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-6-3330T>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50008605 | |||||||
chr13:50008835 | G | A | 2 | a0001c0001t0037g0044 a0001c0001t0108g0044 |
2 | NA18955.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-6-3100G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50008835 | |||||||
chr13:50008852 | C | CA | 7 | a0001c0001t0026g0128 a0001c0001t0044g0124 a0001c0001t0053g0019 others(4): Show |
8 | HG01361.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-3074dupA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50008852 | ||||||
chr13:50008889 | T | C | 6 | a0001c0001t0001g0012 a0001c0001t0008g0012 a0001c0001t0008g0168 others(3): Show |
8 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-3046T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50008889 | |||||||
chr13:50008918 | A | C | 43 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0101 others(40): Show |
48 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-6-3017A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50008918 | |||||||
chr13:50009020 | C | CA | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(128): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-6-2892dupA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009020 | ||||||
chr13:50009020 | C | CAA | 12 | a0001c0001t0003g0101 a0001c0001t0003g0116 a0001c0001t0005g0112 others(9): Show |
12 | HG02055.hp2 HG02056.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6-2893_-6-2892dup others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009020 | ||||||
chr13:50009020 | CA | C | 21 | a0001c0001t0002g0134 a0001c0001t0004g0032 a0001c0001t0004g0068 others(18): Show |
22 | HG01074.hp1 HG01106.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.-6-2892delA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009020 | ||||||
chr13:50009020 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0106g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-6-2902_-6-2892del others(11): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009020 | ||||||
chr13:50009020 | CAAAAAAA others(5): Show |
C | 10 | a0002c0002t0054g0050 a0002c0002t0063g0193 a0002c0002t0165g0018 others(7): Show |
11 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-6-2903_-6-2892del others(12): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009020 | ||||||
chr13:50009116 | TACTC | T | 52 | a0001c0001t0004g0006 a0001c0001t0004g0032 a0001c0001t0004g0062 others(49): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.-6-2816_-6-2813del others(4): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009116 | ||||||
chr13:50009118 | C | CGTAAAAT others(1940): Show |
1 | a0001c0001t0009g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-6-2817_-6-2816ins others(1947): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009118 | |||||||
chr13:50009119 | T | A | 1 | a0001c0001t0009g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-6-2816T>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009119 | |||||||
chr13:50009120 | C | T | 1 | a0001c0001t0009g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-6-2815C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009120 | |||||||
chr13:50009122 | C | T | 1 | a0001c0001t0194g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-6-2813C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009122 | |||||||
chr13:50009238 | C | G | 1 | a0001c0001t0035g0178 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-6-2697C>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009238 | |||||||
chr13:50009276 | C | T | 1 | a0001c0001t0007g0177 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-6-2659C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009276 | |||||||
chr13:50009319 | C | T | 1 | a0001c0001t0042g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-6-2616C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009319 | |||||||
chr13:50009320 | G | A | 1 | a0001c0001t0184g0089 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-6-2615G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009320 | |||||||
chr13:50009383 | C | T | 1 | a0001c0001t0005g0112 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-6-2552C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009383 | |||||||
chr13:50009462 | C | G | 1 | a0001c0001t0003g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-6-2473C>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009462 | |||||||
chr13:50009464 | C | T | 1 | a0001c0001t0180g0066 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-6-2471C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009464 | |||||||
chr13:50009507 | C | T | 10 | a0002c0002t0054g0050 a0002c0002t0063g0193 a0002c0002t0165g0018 others(7): Show |
11 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-6-2428C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009507 | |||||||
chr13:50009512 | G | T | 1 | a0001c0001t0008g0176 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-6-2423G>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009512 | |||||||
chr13:50009576 | A | C | 86 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
98 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-6-2359A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009576 | |||||||
chr13:50009626 | A | G | 10 | a0002c0002t0054g0050 a0002c0002t0063g0193 a0002c0002t0165g0018 others(7): Show |
11 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-6-2309A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009626 | |||||||
chr13:50009736 | C | CA | 49 | a0001c0001t0002g0008 a0001c0001t0002g0022 a0001c0001t0003g0003 others(46): Show |
59 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.-6-2177dupA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009736 | ||||||
chr13:50009736 | C | CAA | 21 | a0001c0001t0002g0113 a0001c0001t0003g0017 a0001c0001t0003g0116 others(18): Show |
22 | HG00423.hp1 HG01255.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-6-2178_-6-2177dup others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009736 | ||||||
chr13:50009736 | CA | C | 45 | a0001c0001t0002g0040 a0001c0001t0002g0130 a0001c0001t0002g0134 others(42): Show |
58 | HG00621.hp2 HG00733.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.-6-2177delA | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009736 | ||||||
chr13:50009747 | A | C | 16 | a0001c0001t0053g0019 a0001c0001t0168g0019 a0001c0001t0173g0196 others(13): Show |
18 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-6-2188A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009747 | |||||||
chr13:50009751 | A | AAC | 20 | a0001c0001t0001g0004 a0001c0001t0001g0169 a0001c0001t0001g0182 others(17): Show |
22 | HG00673.hp2 HG01175.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.-6-2183_-6-2182ins others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009751 | ||||||
chr13:50009751 | A | AC | 56 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0090 others(53): Show |
73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-6-2184_-6-2183ins others(1): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009751 | |||||||
chr13:50009753 | A | AC | 3 | a0001c0001t0023g0150 a0001c0001t0046g0080 a0001c0001t0123g0074 |
3 | HG00735.hp1 HG02523.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-6-2182_-6-2181ins others(1): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009753 | |||||||
chr13:50009753 | A | C | 1 | a0001c0001t0201g0187 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-6-2182A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009753 | |||||||
chr13:50009754 | A | C | 41 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(38): Show |
54 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.-6-2181A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009754 | |||||||
chr13:50009756 | A | AAC | 13 | a0001c0001t0004g0062 a0001c0001t0004g0069 a0001c0001t0017g0087 others(10): Show |
13 | HG01069.hp1 HG01123.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-2178_-6-2177ins others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50009756 | ||||||
chr13:50009756 | A | AC | 44 | a0001c0001t0003g0149 a0001c0001t0004g0006 a0001c0001t0004g0032 others(41): Show |
53 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.-6-2179_-6-2178ins others(1): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009756 | |||||||
chr13:50009756 | A | C | 2 | a0001c0001t0046g0080 a0001c0001t0123g0074 |
2 | HG00735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-6-2179A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009756 | |||||||
chr13:50009798 | G | A | 1 | a0001c0001t0016g0135 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-6-2137G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009798 | |||||||
chr13:50009867 | T | C | 1 | a0001c0001t0019g0091 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-6-2068T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009867 | |||||||
chr13:50009967 | A | G | 1 | a0001c0001t0007g0175 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-6-1968A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50009967 | |||||||
chr13:50010015 | A | G | 42 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(39): Show |
55 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-6-1920A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010015 | |||||||
chr13:50010040 | C | CT | 62 | a0001c0001t0001g0172 a0001c0001t0002g0022 a0001c0001t0002g0040 others(59): Show |
63 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.-6-1872dupT | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50010040 | ||||||
chr13:50010040 | C | CTT | 9 | a0001c0001t0002g0130 a0001c0001t0003g0149 a0001c0001t0011g0126 others(6): Show |
9 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.-6-1873_-6-1872dup others(2): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50010040 | ||||||
chr13:50010040 | CTTTT | C | 37 | a0001c0001t0010g0005 a0001c0001t0014g0014 a0001c0001t0014g0186 others(34): Show |
49 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-6-1875_-6-1872del others(4): Show |
TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 50010040 | ||||||
chr13:50010062 | T | C | 1 | a0001c0001t0194g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-6-1873T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010062 | |||||||
chr13:50010063 | T | C | 26 | a0001c0001t0010g0005 a0001c0001t0010g0028 a0001c0001t0014g0014 others(23): Show |
37 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-6-1872T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010063 | |||||||
chr13:50010064 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-6-1871C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010064 | |||||||
chr13:50010207 | G | A | 86 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
98 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-6-1728G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010207 | |||||||
chr13:50010334 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-6-1601G>A | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010334 | |||||||
chr13:50010448 | T | C | 6 | a0001c0001t0002g0015 a0001c0001t0011g0015 a0001c0001t0011g0126 others(3): Show |
8 | HG00544.hp1 HG00621.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-1487T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010448 | |||||||
chr13:50010456 | T | G | 1 | a0001c0001t0002g0134 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-6-1479T>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010456 | |||||||
chr13:50010467 | C | T | 2 | a0001c0001t0004g0064 a0001c0001t0004g0068 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-6-1468C>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010467 | |||||||
chr13:50010561 | A | T | 3 | a0001c0001t0004g0062 a0001c0001t0004g0069 a0001c0001t0070g0063 |
3 | HG00323.hp2 HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-6-1374A>T | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010561 | |||||||
chr13:50010687 | T | C | 2 | a0001c0001t0136g0042 a0001c0001t0185g0042 |
2 | HG02683.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-6-1248T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010687 | |||||||
chr13:50010694 | A | G | 2 | a0001c0001t0136g0042 a0001c0001t0185g0042 |
2 | HG02683.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-6-1241A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50010694 | |||||||
chr13:50011003 | A | G | 1 | a0001c0001t0150g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-6-932A>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50011003 | |||||||
chr13:50011061 | T | C | 1 | a0001c0001t0005g0114 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-6-874T>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50011061 | |||||||
chr13:50011629 | T | G | 1 | a0001c0001t0024g0107 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-6-306T>G | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50011629 | |||||||
chr13:50011735 | A | C | 1 | a0001c0001t0080g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-6-200A>C | TRIM13 | ENSG00000204977.10 | transcript | ENST00000378182.4 | protein_coding | 1/1 | chr13 | 50011735 |