Variant report

Variant rs9587991
Chromosome Location chr13:110468395-110468396
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:110455800-110469200 Weak transcription Pancreas Pancrea
2 chr13:110463400-110468800 Weak transcription NH-A brain
3 chr13:110463600-110468600 Weak transcription Muscle Satellite Cultured Cells --
4 chr13:110463600-110468800 Weak transcription HSMMtube muscle
5 chr13:110463800-110469200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr13:110464200-110468400 Weak transcription HSMM muscle
7 chr13:110465600-110468600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr13:110465600-110469600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr13:110465600-110469800 Weak transcription Fetal Muscle Trunk muscle
10 chr13:110466400-110469000 Weak transcription Stomach Smooth Muscle stomach
11 chr13:110467400-110469200 Enhancers Dnd41 blood
12 chr13:110468200-110468400 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr13:110468200-110469200 Flanking Active TSS Liver Liver
14 chr13:110468200-110469200 Enhancers Pancreatic Islets Pancreatic Islet
15 chr13:110468200-110469600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr13:110468200-110469800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
17 chr13:110468200-110470400 Enhancers ES-I3 Cell Line embryonic stem cell
18 chr13:110468200-110470400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
19 chr13:110468200-110471000 Enhancers Cortex derived primary cultured neurospheres brain

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