Variant report

Variant rs1515309
Chromosome Location chr2:180444967-180444968
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180433000-180445600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr2:180435200-180461000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:180435400-180446400 Weak transcription Fetal Kidney kidney
4 chr2:180437600-180445200 Weak transcription Skeletal Muscle Male skeletal muscle
5 chr2:180439400-180445000 Weak transcription Stomach Mucosa stomach
6 chr2:180439800-180445200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr2:180439800-180445200 Weak transcription Fetal Lung lung
8 chr2:180439800-180446400 Enhancers Liver Liver
9 chr2:180441200-180445200 Weak transcription Pancreas Pancrea
10 chr2:180442400-180446800 Enhancers HepG2 liver
11 chr2:180443600-180445000 Weak transcription Fetal Intestine Large intestine
12 chr2:180444200-180445200 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr2:180444200-180445800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr2:180444600-180445200 Enhancers Adipose Nuclei Adipose
15 chr2:180444600-180445800 Enhancers Fetal Intestine Small intestine
16 chr2:180444800-180445800 Enhancers Breast Myoepithelial Primary Cells Breast

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