Variant report

Variant rs10915713
Chromosome Location chr1:224954067-224954068
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
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

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