Variant report

Variant rs2305428
Chromosome Location chr2:209001699-209001700
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:208993400-209002200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr2:208994600-209002200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr2:208998800-209002000 Enhancers Fetal Intestine Small intestine
4 chr2:208998800-209002400 Enhancers Fetal Intestine Large intestine
5 chr2:208999200-209002200 Enhancers HepG2 liver
6 chr2:208999600-209002000 Enhancers Ovary ovary
7 chr2:208999600-209002000 Enhancers Stomach Mucosa stomach
8 chr2:209000400-209001800 Enhancers Pancreatic Islets Pancreatic Islet
9 chr2:209000600-209001800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:209000800-209001800 Enhancers Duodenum Mucosa Duodenum
11 chr2:209001400-209001800 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr2:209001400-209003000 Enhancers HMEC breast
13 chr2:209001600-209002400 Enhancers Placenta Placenta

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