Variant report

Variant rs66901908
Chromosome Location chr3:155974630-155974631
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:155970000-155977400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr3:155971800-155976400 Weak transcription Aorta Aorta
3 chr3:155973400-155976200 Weak transcription Fetal Heart heart
4 chr3:155974200-155975400 Enhancers NHEK skin
5 chr3:155974200-155975600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr3:155974200-155976200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr3:155974400-155975000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr3:155974400-155977400 Weak transcription HUVEC blood vessel

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