Variant report

Variant rs186839162
Chromosome Location chr12:50350478-50350479
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:50339400-50353600 Weak transcription Right Atrium heart
2 chr12:50347400-50353400 Weak transcription Pancreas Pancrea
3 chr12:50348400-50350800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr12:50348800-50350800 Bivalent Enhancer Primary hematopoietic stem cells blood
5 chr12:50349200-50350800 Bivalent Enhancer Primary monocytes fromperipheralblood blood
6 chr12:50349600-50350600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr12:50349600-50353400 Weak transcription Spleen Spleen
8 chr12:50349800-50350600 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
9 chr12:50350200-50350800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr12:50350200-50352800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr12:50350400-50350600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr12:50350400-50350600 Flanking Bivalent TSS/Enh Primary neutrophils fromperipheralblood blood
13 chr12:50350400-50350600 Flanking Bivalent TSS/Enh Primary hematopoietic stem cells short term culture blood
14 chr12:50350400-50350600 Bivalent Enhancer Primary mononuclear cells fromperipheralblood Blood
15 chr12:50350400-50350800 Weak transcription Hela-S3 cervix

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