Variant report

Variant rs35432937
Chromosome Location chr4:8336769-8336770
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:8325600-8338400 Weak transcription Placenta Amnion Placenta Amnion
2 chr4:8333000-8336800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr4:8333400-8342400 Weak transcription Psoas Muscle Psoas
4 chr4:8333400-8342400 Weak transcription Right Atrium heart
5 chr4:8334600-8336800 Weak transcription Right Ventricle heart
6 chr4:8334800-8337800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr4:8335000-8337600 Weak transcription HMEC breast
8 chr4:8335000-8338000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr4:8335000-8338400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr4:8336600-8336800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr4:8336600-8336800 Bivalent Enhancer Fetal Muscle Trunk muscle
12 chr4:8336600-8337200 Flanking Active TSS HepG2 liver
13 chr4:8336600-8337400 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr4:8336600-8337400 Enhancers Pancreas Pancrea

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