Variant report

Variant rs4742765
Chromosome Location chr9:102029531-102029532
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:102022200-102034800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr9:102022200-102038000 Weak transcription Aorta Aorta
3 chr9:102028200-102029600 Enhancers Fetal Thymus thymus
4 chr9:102028400-102029600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
5 chr9:102028600-102029600 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr9:102028600-102029600 Flanking Active TSS GM12878-XiMat blood
7 chr9:102028600-102029600 Enhancers NHDF-Ad bronchial
8 chr9:102028800-102029600 Enhancers Thymus Thymus
9 chr9:102028800-102029600 Enhancers NH-A brain
10 chr9:102028800-102029600 Enhancers NHLF lung
11 chr9:102029000-102030800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr9:102029000-102031000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr9:102029200-102031000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr9:102029400-102029600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr9:102029400-102030600 Weak transcription HUVEC blood vessel
16 chr9:102029400-102031000 Weak transcription Osteobl bone
17 chr9:102029400-102031400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr9:102029400-102034600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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