Variant report

Variant rs73795838
Chromosome Location chr4:3673472-3673473
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3658600-3678000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr4:3669400-3693400 Weak transcription Right Atrium heart
3 chr4:3670000-3677600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr4:3670800-3674000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr4:3672800-3675600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr4:3673000-3674000 Enhancers HepG2 liver
7 chr4:3673000-3674200 Enhancers Pancreas Pancrea
8 chr4:3673000-3674600 Enhancers Lung lung
9 chr4:3673200-3673800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
10 chr4:3673400-3673600 Enhancers Brain Anterior Caudate brain
11 chr4:3673400-3674000 Enhancers A549 lung
12 chr4:3673400-3674200 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
13 chr4:3673400-3674200 Bivalent Enhancer Fetal Stomach stomach
14 chr4:3673400-3674200 Enhancers Gastric stomach

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