Variant report

Variant rs7983700
Chromosome Location chr13:51635688-51635689
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:51632600-51639800 Enhancers Brain Germinal Matrix brain
2 chr13:51632800-51639200 Weak transcription Spleen Spleen
3 chr13:51633200-51637400 Weak transcription Fetal Brain Male brain
4 chr13:51633200-51639400 Weak transcription Fetal Muscle Leg muscle
5 chr13:51633200-51639800 Weak transcription Fetal Stomach stomach
6 chr13:51633200-51641000 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr13:51633400-51638800 Weak transcription Fetal Lung lung
8 chr13:51633400-51657800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr13:51633800-51640000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr13:51633800-51640800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr13:51634000-51637600 Weak transcription Primary hematopoietic stem cells short term culture blood
12 chr13:51634200-51636800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr13:51634400-51636200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr13:51634400-51640800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr13:51634600-51637000 Weak transcription Primary hematopoietic stem cells blood

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