Variant report

Variant rs2271867
Chromosome Location chr9:139946804-139946805
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr9:139945800-139947400 Bivalent Enhancer Fetal Muscle Leg muscle
9 chr9:139946000-139947800 Weak transcription Gastric stomach
10 chr9:139946200-139947400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
11 chr9:139946200-139947600 Bivalent Enhancer Fetal Muscle Trunk muscle
12 chr9:139946600-139947200 Bivalent/Poised TSS iPS DF 19.11 Cell Line embryonic stem cell
13 chr9:139946600-139947400 Bivalent Enhancer Primary neutrophils fromperipheralblood blood
14 chr9:139946800-139947200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
15 chr9:139946800-139947800 Bivalent Enhancer Primary T helper 17 cells PMA-I stimulated --

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