Variant report

Variant rs12477555
Chromosome Location chr2:172033165-172033166
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:172030600-172035600 Weak transcription GM12878-XiMat blood
2 chr2:172031600-172036800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:172031600-172036800 Weak transcription NHEK skin
4 chr2:172031600-172037000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:172031800-172033400 Weak transcription Placenta Placenta
6 chr2:172032800-172033200 Bivalent Enhancer HepG2 liver
7 chr2:172032800-172033400 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr2:172032800-172033400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr2:172032800-172033600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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