Variant report

Variant rs663806
Chromosome Location chr6:113706059-113706060
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:113699200-113706400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr6:113703400-113706200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr6:113703600-113706200 Weak transcription HUVEC blood vessel
4 chr6:113703600-113706400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr6:113703800-113706400 Weak transcription Fetal Lung lung
6 chr6:113704600-113712000 Weak transcription Fetal Stomach stomach
7 chr6:113704800-113706600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr6:113705000-113706200 Weak transcription Osteobl bone
9 chr6:113705000-113708600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr6:113705600-113707400 Enhancers NHDF-Ad bronchial
11 chr6:113705800-113706400 Enhancers Muscle Satellite Cultured Cells --
12 chr6:113705800-113707000 Enhancers NH-A brain
13 chr6:113705800-113707200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr6:113705800-113707400 Enhancers HSMM muscle
15 chr6:113706000-113707000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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