Variant report
Variant | rs7581496 |
---|---|
Chromosome Location | chr2:33930328-33930329 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:33928800-33930400 | Enhancers | HUES64 Cell Line | embryonic stem cell |
2 | chr2:33929000-33930400 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr2:33929000-33931800 | Enhancers | Cortex derived primary cultured neurospheres | brain |
4 | chr2:33929200-33930400 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
5 | chr2:33929200-33930600 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
6 | chr2:33929400-33930400 | Enhancers | HUES6 Cell Line | embryonic stem cell |
7 | chr2:33930000-33930600 | Enhancers | HUVEC | blood vessel |
8 | chr2:33930000-33932000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
9 | chr2:33930000-33937400 | Weak transcription | H9 Cell Line | embryonic stem cell |
10 | chr2:33930200-33937000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
11 | chr2:33930200-33937000 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |