Variant report

Variant rs567296170
Chromosome Location chr12:50345455-50345456
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:50339400-50353600 Weak transcription Right Atrium heart
2 chr12:50340200-50346000 Weak transcription Lung lung
3 chr12:50342400-50346000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr12:50343200-50345800 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
5 chr12:50344000-50347800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr12:50344600-50347600 Enhancers Spleen Spleen
7 chr12:50344800-50346200 Weak transcription Stomach Mucosa stomach
8 chr12:50345000-50346200 Weak transcription Pancreas Pancrea
9 chr12:50345000-50346400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
10 chr12:50345000-50346800 Active TSS Fetal Kidney kidney
11 chr12:50345200-50347400 Bivalent Enhancer Primary monocytes fromperipheralblood blood
12 chr12:50345400-50347200 Enhancers Hela-S3 cervix
13 chr12:50345400-50347200 Bivalent Enhancer Monocytes-CD14+_RO01746 blood

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