Variant report

Variant rs2856923
Chromosome Location chr9:116838728-116838729
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 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 chr9:116835400-116839000 Weak transcription Stomach Mucosa stomach
4 chr9:116835400-116840200 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr9:116836200-116838800 Transcr. at gene 5' and 3' HepG2 liver
6 chr9:116837000-116839200 Enhancers Pancreas Pancrea
7 chr9:116837200-116842400 Enhancers A549 lung
8 chr9:116838400-116838800 Flanking Active TSS Liver Liver
9 chr9:116838600-116839000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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