Variant report

Variant rs7687802
Chromosome Location chr4:175316854-175316855
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:175312400-175318200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr4:175315400-175317200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr4:175315600-175317000 Enhancers Muscle Satellite Cultured Cells --
4 chr4:175316000-175320000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr4:175316000-175320200 Weak transcription NH-A brain
6 chr4:175316200-175317000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr4:175316200-175319800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr4:175316200-175319800 Weak transcription NHLF lung
9 chr4:175316600-175317000 Flanking Active TSS A549 lung
10 chr4:175316800-175317800 Enhancers NHDF-Ad bronchial

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