Variant report

Variant rs2719209
Chromosome Location chr8:130427651-130427652
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:130410200-130434600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr8:130425000-130427800 Weak transcription Fetal Stomach stomach
3 chr8:130426400-130428400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr8:130426600-130428400 Enhancers Primary monocytes fromperipheralblood blood
5 chr8:130426600-130430800 Genic enhancers K562 blood
6 chr8:130426800-130428000 Weak transcription Primary hematopoietic stem cells blood
7 chr8:130426800-130428600 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr8:130427000-130428400 Enhancers Monocytes-CD14+_RO01746 blood
9 chr8:130427000-130449000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr8:130427400-130429400 Flanking Active TSS Dnd41 blood
11 chr8:130427600-130428000 Enhancers Adipose Nuclei Adipose
12 chr8:130427600-130428000 Flanking Active TSS Thymus Thymus
13 chr8:130427600-130428200 Enhancers GM12878-XiMat blood
14 chr8:130427600-130428400 Flanking Active TSS Fetal Thymus thymus
15 chr8:130427600-130429000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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