Variant report

Variant rs9483389
Chromosome Location chr6:132468518-132468519
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132459600-132494800 Weak transcription Primary B cells from cord blood blood
2 chr6:132467200-132470000 Strong transcription HUVEC blood vessel
3 chr6:132467400-132470000 Enhancers NHDF-Ad bronchial
4 chr6:132467600-132471000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr6:132467800-132468600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr6:132467800-132470000 Enhancers Osteobl bone
7 chr6:132467800-132470200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr6:132468000-132469800 Enhancers NHLF lung
9 chr6:132468000-132470000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr6:132468200-132468600 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr6:132468200-132468800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr6:132468200-132469000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr6:132468200-132469200 Enhancers Fetal Muscle Leg muscle
14 chr6:132468200-132469400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr6:132468200-132469600 Enhancers Muscle Satellite Cultured Cells --
16 chr6:132468200-132469800 Enhancers Fetal Stomach stomach
17 chr6:132468200-132469800 Enhancers HSMMtube muscle
18 chr6:132468200-132469800 Enhancers NH-A brain
19 chr6:132468400-132470000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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