Variant report

Variant rs374844138
Chromosome Location chr12:50350274-50350275
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr12:50348800-50350400 Bivalent Enhancer Fetal Stomach stomach
5 chr12:50348800-50350800 Bivalent Enhancer Primary hematopoietic stem cells blood
6 chr12:50349200-50350400 Bivalent Enhancer Primary neutrophils fromperipheralblood blood
7 chr12:50349200-50350800 Bivalent Enhancer Primary monocytes fromperipheralblood blood
8 chr12:50349600-50350600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr12:50349600-50353400 Weak transcription Spleen Spleen
10 chr12:50349800-50350400 Enhancers Hela-S3 cervix
11 chr12:50349800-50350600 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
12 chr12:50350000-50350400 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
13 chr12:50350200-50350400 Bivalent Enhancer GM12878-XiMat blood
14 chr12:50350200-50350400 Bivalent Enhancer Monocytes-CD14+_RO01746 blood
15 chr12:50350200-50350800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr12:50350200-50352800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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