Variant report

Variant rs8009939
Chromosome Location chr14:21657896-21657897
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:21651200-21659600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr14:21654200-21659200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr14:21654200-21659400 Weak transcription Primary hematopoietic stem cells blood
4 chr14:21654200-21659400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr14:21654800-21659400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr14:21656200-21660000 Weak transcription Placenta Amnion Placenta Amnion
7 chr14:21656400-21660000 Weak transcription H9 Cell Line embryonic stem cell
8 chr14:21656800-21659600 Weak transcription Lung lung
9 chr14:21657400-21658000 Enhancers HepG2 liver

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