Variant report

Variant rs10870190
Chromosome Location chr9:140025227-140025228
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140021800-140025400 Active TSS A549 lung
2 chr9:140023200-140025600 Active TSS Rectal Smooth Muscle rectum
3 chr9:140023400-140025400 Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
4 chr9:140023600-140025400 Enhancers Fetal Brain Male brain
5 chr9:140023600-140025600 Active TSS H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr9:140023600-140025800 Active TSS Hela-S3 cervix
7 chr9:140024800-140025400 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
8 chr9:140024800-140025400 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr9:140024800-140025400 Flanking Active TSS Foreskin Melanocyte Primary Cells skin03 Skin
10 chr9:140025000-140025400 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
11 chr9:140025000-140025600 Active TSS Primary T helper naive cells from peripheral blood blood
12 chr9:140025000-140025600 Bivalent Enhancer Fetal Thymus thymus
13 chr9:140025000-140033400 Weak transcription Right Atrium heart
14 chr9:140025200-140025400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr9:140025200-140025400 Active TSS H9 Derived Neuron Cultured Cells ES cell derived
16 chr9:140025200-140025400 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
17 chr9:140025200-140025400 Bivalent/Poised TSS iPS DF 19.11 Cell Line embryonic stem cell
18 chr9:140025200-140025400 Bivalent Enhancer Primary T cells fromperipheralblood blood
19 chr9:140025200-140025400 Enhancers Primary hematopoietic stem cells short term culture blood
20 chr9:140025200-140025400 Active TSS GM12878-XiMat blood
21 chr9:140025200-140025600 Active TSS Esophagus oesophagus
22 chr9:140025200-140026200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
23 chr9:140025200-140026200 Weak transcription K562 blood

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