Variant report
Variant | rs71418693 |
---|---|
Chromosome Location | chr2:209360727-209360728 |
allele | A/G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:209355200-209361000 | Weak transcription | Stomach Mucosa | stomach |
2 | chr2:209355200-209366000 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
3 | chr2:209356600-209361000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr2:209360000-209361000 | Enhancers | HUES64 Cell Line | embryonic stem cell |
5 | chr2:209360000-209361200 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
6 | chr2:209360200-209361200 | Enhancers | H1 Cell Line | embryonic stem cell |
7 | chr2:209360200-209361200 | Enhancers | HUES6 Cell Line | embryonic stem cell |
8 | chr2:209360200-209361400 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
9 | chr2:209360200-209361600 | Enhancers | HUES48 Cell Line | embryonic stem cell |
10 | chr2:209360400-209361200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
11 | chr2:209360600-209360800 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |