Variant report

Variant rs11708961
Chromosome Location chr3:105681416-105681417
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:105677600-105689400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr3:105677800-105684400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:105679400-105683600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr3:105680800-105682600 Enhancers HepG2 liver
5 chr3:105681200-105682000 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr3:105681200-105682400 Enhancers Right Atrium heart
7 chr3:105681200-105682400 Enhancers Stomach Mucosa stomach
8 chr3:105681200-105682400 Enhancers Hela-S3 cervix
9 chr3:105681400-105681800 Enhancers Pancreas Pancrea
10 chr3:105681400-105681800 Enhancers Osteobl bone
11 chr3:105681400-105682000 Enhancers HUVEC blood vessel

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