Variant report

Variant rs7667642
Chromosome Location chr4:175317355-175317356
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 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 chr4:175316000-175320000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr4:175316000-175320200 Weak transcription NH-A brain
4 chr4:175316200-175319800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:175316200-175319800 Weak transcription NHLF lung
6 chr4:175316800-175317800 Enhancers NHDF-Ad bronchial
7 chr4:175317000-175317400 Weak transcription Muscle Satellite Cultured Cells --
8 chr4:175317000-175317600 Enhancers A549 lung
9 chr4:175317200-175319600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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