Variant report
Variant | rs10177258 |
---|---|
Chromosome Location | chr2:212475632-212475633 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:212467200-212480000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
2 | chr2:212467400-212546800 | Weak transcription | Aorta | Aorta |
3 | chr2:212470400-212489600 | Weak transcription | Fetal Heart | heart |
4 | chr2:212473600-212476200 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
5 | chr2:212474600-212476000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
6 | chr2:212475200-212476400 | Enhancers | HUES6 Cell Line | embryonic stem cell |
7 | chr2:212475400-212475800 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
8 | chr2:212475600-212475800 | Enhancers | HepG2 | liver |
9 | chr2:212475600-212477400 | Flanking Active TSS | Dnd41 | blood |