Variant report
Variant | rs545208283 |
---|---|
Chromosome Location | chr10:118766632-118766633 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:118765400-118766800 | Enhancers | Primary monocytes fromperipheralblood | blood |
2 | chr10:118765600-118766800 | Enhancers | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
3 | chr10:118765600-118766800 | Enhancers | HUVEC | blood vessel |
4 | chr10:118765600-118767000 | Enhancers | Brain Substantia Nigra | brain |
5 | chr10:118765600-118767200 | Enhancers | Monocytes-CD14+_RO01746 | blood |
6 | chr10:118765800-118766800 | Enhancers | HepG2 | liver |
7 | chr10:118766200-118766800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
8 | chr10:118766200-118767200 | Flanking Active TSS | A549 | lung |
9 | chr10:118766400-118766800 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
10 | chr10:118766600-118766800 | Enhancers | HUES48 Cell Line | embryonic stem cell |
11 | chr10:118766600-118767200 | Enhancers | K562 | blood |
12 | chr10:118766600-118768200 | Weak transcription | Brain Hippocampus Middle | brain |