Variant report

Variant rs373974439
Chromosome Location chr12:31206189-31206190
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31189800-31225400 Weak transcription Fetal Stomach stomach
2 chr12:31195000-31206200 Weak transcription Left Ventricle heart
3 chr12:31202200-31219400 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr12:31203200-31207600 Enhancers Fetal Thymus thymus
5 chr12:31204200-31206800 Enhancers Thymus Thymus
6 chr12:31205000-31206200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr12:31205000-31206200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr12:31205000-31206400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr12:31205000-31210400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr12:31205400-31207000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr12:31205400-31207000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr12:31205600-31206200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr12:31205800-31206200 Weak transcription HSMMtube muscle
14 chr12:31206000-31206200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr12:31206000-31206600 Enhancers NH-A brain
16 chr12:31206000-31206800 Enhancers HepG2 liver
17 chr12:31206000-31207000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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