Variant report

Variant rs6721295
Chromosome Location chr2:180443963-180443964
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180433000-180445600 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 chr2:180443200-180444200 Enhancers Pancreatic Islets Pancreatic Islet
12 chr2:180443600-180444600 Weak transcription Fetal Intestine Small intestine
13 chr2:180443600-180445000 Weak transcription Fetal Intestine Large intestine

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