Variant report

Variant rs4880212
Chromosome Location chr9:140025595-140025596
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140023200-140025600 Active TSS Rectal Smooth Muscle rectum
2 chr9:140023600-140025600 Active TSS H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr9:140023600-140025800 Active TSS Hela-S3 cervix
4 chr9:140025000-140025600 Active TSS Primary T helper naive cells from peripheral blood blood
5 chr9:140025000-140025600 Bivalent Enhancer Fetal Thymus thymus
6 chr9:140025000-140033400 Weak transcription Right Atrium heart
7 chr9:140025200-140025600 Active TSS Esophagus oesophagus
8 chr9:140025200-140026200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr9:140025200-140026200 Weak transcription K562 blood
10 chr9:140025400-140025600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr9:140025400-140025600 Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr9:140025400-140025600 Flanking Active TSS GM12878-XiMat blood
13 chr9:140025400-140025800 Weak transcription Primary hematopoietic stem cells short term culture blood
14 chr9:140025400-140031200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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