Variant report

Variant rs12533963
Chromosome Location chr7:66091096-66091097
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:66086800-66092800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr7:66087600-66092200 Weak transcription K562 blood
3 chr7:66087600-66092800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr7:66089800-66092800 Enhancers Placenta Placenta
5 chr7:66090200-66091800 Enhancers HepG2 liver
6 chr7:66090200-66092800 Weak transcription Stomach Mucosa stomach
7 chr7:66090400-66092200 Enhancers NHDF-Ad bronchial
8 chr7:66090400-66092800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr7:66090600-66092200 Enhancers Colon Smooth Muscle Colon
10 chr7:66090600-66093000 Enhancers NHLF lung
11 chr7:66090800-66091400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr7:66090800-66092800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr7:66091000-66091800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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