Variant report

Variant rs368807998
Chromosome Location chr9:116839030-116839031
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116834600-116839800 Weak transcription Fetal Intestine Small intestine
2 chr9:116834800-116839600 Weak transcription Gastric stomach
3 chr9:116835400-116840200 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr9:116837000-116839200 Enhancers Pancreas Pancrea
5 chr9:116837200-116842400 Enhancers A549 lung
6 chr9:116838800-116840600 Active TSS Liver Liver
7 chr9:116838800-116840600 Bivalent/Poised TSS HepG2 liver
8 chr9:116839000-116839800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:116839000-116841600 Enhancers Rectal Mucosa Donor 31 rectum
10 chr9:116839000-116845200 Enhancers Stomach Mucosa stomach

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