Variant report

Variant rs4880084
Chromosome Location chr9:139946327-139946328
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139941200-139947800 Weak transcription Right Atrium heart
2 chr9:139944400-139948200 Weak transcription K562 blood
3 chr9:139944600-139947200 Weak transcription Liver Liver
4 chr9:139944800-139947200 Weak transcription HMEC breast
5 chr9:139944800-139947400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr9:139944800-139947600 Weak transcription Pancreas Pancrea
7 chr9:139945400-139947400 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr9:139945800-139946600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:139945800-139947400 Bivalent Enhancer Fetal Muscle Leg muscle
10 chr9:139946000-139947800 Weak transcription Gastric stomach
11 chr9:139946200-139947400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
12 chr9:139946200-139947600 Bivalent Enhancer Fetal Muscle Trunk muscle

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