Variant report

Variant rs4901641
Chromosome Location chr14:56633025-56633026
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:56615600-56639800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr14:56616800-56640200 Weak transcription Fetal Stomach stomach
3 chr14:56621400-56637600 Weak transcription Small Intestine intestine
4 chr14:56627200-56633400 Weak transcription Thymus Thymus
5 chr14:56627200-56634400 Weak transcription Pancreas Pancrea
6 chr14:56627200-56645000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr14:56627400-56634400 Weak transcription Stomach Mucosa stomach
8 chr14:56628200-56633400 Weak transcription Fetal Thymus thymus
9 chr14:56632200-56638000 Enhancers Dnd41 blood
10 chr14:56632400-56633400 ZNF genes & repeats Primary T cells from cord blood blood

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