Variant report

Variant rs17079086
Chromosome Location chr6:117674158-117674159
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:117644200-117676000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr6:117650400-117700000 Weak transcription HSMM muscle
3 chr6:117662000-117717200 Weak transcription HSMMtube muscle
4 chr6:117668000-117675400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr6:117668200-117686800 Weak transcription Osteobl bone
6 chr6:117672400-117674200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr6:117673800-117674200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr6:117673800-117674200 Enhancers Hela-S3 cervix
9 chr6:117673800-117674400 Enhancers Fetal Intestine Small intestine
10 chr6:117673800-117674400 Enhancers Stomach Mucosa stomach
11 chr6:117673800-117674400 Enhancers HMEC breast
12 chr6:117674000-117676400 Enhancers Fetal Intestine Large intestine

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