Variant report

Variant rs16898978
Chromosome Location chr8:124893112-124893113
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:124888200-124893800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr8:124889400-124894600 Weak transcription Right Atrium heart
3 chr8:124891000-124893400 Weak transcription Osteobl bone
4 chr8:124891400-124893200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr8:124891400-124893600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr8:124891400-124893800 Weak transcription Adipose Nuclei Adipose
7 chr8:124891600-124893800 Weak transcription Fetal Muscle Leg muscle
8 chr8:124892200-124893400 Weak transcription NHDF-Ad bronchial
9 chr8:124892400-124894200 Enhancers Fetal Intestine Large intestine
10 chr8:124892600-124893200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
11 chr8:124892600-124893400 Enhancers Hela-S3 cervix
12 chr8:124893000-124893200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr8:124893000-124893200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr8:124893000-124893800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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