Variant report

Variant rs4741684
Chromosome Location chr9:2356359-2356360
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:2354800-2356600 Enhancers NHEK skin
2 chr9:2355600-2359400 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr9:2355800-2356600 Enhancers HMEC breast
4 chr9:2355800-2359600 Weak transcription Fetal Brain Male brain
5 chr9:2356000-2356600 Weak transcription Fetal Stomach stomach
6 chr9:2356000-2359200 Weak transcription Fetal Lung lung
7 chr9:2356000-2359400 Weak transcription H9 Cell Line embryonic stem cell
8 chr9:2356000-2359400 Weak transcription HUES6 Cell Line embryonic stem cell
9 chr9:2356000-2359400 Weak transcription Fetal Muscle Leg muscle
10 chr9:2356000-2361200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr9:2356000-2362800 Weak transcription Ovary ovary
12 chr9:2356200-2356600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr9:2356200-2359000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived

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