Variant report

Variant rs138918672
Chromosome Location chr12:50350799-50350800
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr12:50349600-50353400 Weak transcription Spleen Spleen
7 chr12:50350200-50350800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr12:50350200-50352800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr12:50350400-50350800 Weak transcription Hela-S3 cervix
10 chr12:50350600-50350800 Bivalent Enhancer Primary neutrophils fromperipheralblood blood
11 chr12:50350600-50352200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr12:50350600-50352400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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