Variant report

Variant rs539293988
Chromosome Location chr12:31206588-31206589
allele -/TG
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31189800-31225400 Weak transcription Fetal Stomach stomach
2 chr12:31202200-31219400 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr12:31203200-31207600 Enhancers Fetal Thymus thymus
4 chr12:31204200-31206800 Enhancers Thymus Thymus
5 chr12:31205000-31210400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr12:31205400-31207000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr12:31205400-31207000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr12:31206000-31206600 Enhancers NH-A brain
9 chr12:31206000-31206800 Enhancers HepG2 liver
10 chr12:31206000-31207000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr12:31206200-31206600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr12:31206200-31206600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr12:31206200-31206600 Enhancers Fetal Intestine Large intestine
14 chr12:31206200-31206800 Enhancers HSMMtube muscle
15 chr12:31206200-31207000 Enhancers Fetal Adrenal Gland Adrenal Gland
16 chr12:31206200-31207000 Enhancers HSMM muscle
17 chr12:31206400-31206600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr12:31206400-31207800 Enhancers Fetal Heart heart

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