Variant report
Variant | rs527894406 |
---|---|
Chromosome Location | chr2:11181011-11181012 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:11180000-11181200 | Enhancers | Cortex derived primary cultured neurospheres | brain |
2 | chr2:11180200-11181200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
3 | chr2:11180200-11181800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
4 | chr2:11180600-11181200 | Enhancers | HUES64 Cell Line | embryonic stem cell |
5 | chr2:11180800-11181400 | Enhancers | HUES48 Cell Line | embryonic stem cell |
6 | chr2:11180800-11181400 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
7 | chr2:11181000-11181400 | Enhancers | ES-WA7 Cell Line | embryonic stem cell |
8 | chr2:11181000-11181400 | Enhancers | H9 Cell Line | embryonic stem cell |
9 | chr2:11181000-11181600 | Enhancers | H1 Cell Line | embryonic stem cell |
10 | chr2:11181000-11182600 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |