Variant report

Variant rs7020933
Chromosome Location chr9:97483009-97483010
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:97479000-97483200 Weak transcription HepG2 liver
2 chr9:97479000-97488400 Weak transcription Fetal Intestine Large intestine
3 chr9:97480000-97483400 Enhancers Placenta Placenta
4 chr9:97480000-97483800 Enhancers NHEK skin
5 chr9:97480000-97484200 Enhancers HMEC breast
6 chr9:97480400-97484200 Weak transcription NHDF-Ad bronchial
7 chr9:97481000-97483800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr9:97481400-97483800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr9:97481400-97484000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr9:97482800-97483200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr9:97483000-97483600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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