Variant report
Variant | rs10915713 |
---|---|
Chromosome Location | chr1:224954067-224954068 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:224944800-224954800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr1:224948000-224956800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
3 | chr1:224953000-224960800 | Weak transcription | Pancreas | Pancrea |
4 | chr1:224953800-224955000 | Enhancers | HUES64 Cell Line | embryonic stem cell |
5 | chr1:224954000-224954200 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
6 | chr1:224954000-224954400 | Enhancers | Fetal Brain Male | brain |
7 | chr1:224954000-224955000 | Enhancers | HUES48 Cell Line | embryonic stem cell |
8 | chr1:224954000-224955800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
9 | chr1:224954000-224956200 | Enhancers | iPS-20b Cell Line | embryonic stem cell |