Variant report

Variant rs7975391
Chromosome Location chr12:1618780-1618781
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:1611600-1618800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr12:1612200-1626000 Weak transcription Muscle Satellite Cultured Cells --
3 chr12:1612800-1621200 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr12:1614200-1626200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr12:1618600-1618800 Bivalent Enhancer Fetal Kidney kidney
6 chr12:1618600-1619000 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr12:1618600-1619400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr12:1618600-1619600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr12:1618600-1619600 Bivalent Enhancer Fetal Muscle Trunk muscle
10 chr12:1618600-1619800 Enhancers Fetal Muscle Leg muscle
11 chr12:1618600-1620400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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