Variant report

Variant rs6576033
Chromosome Location chr14:104852475-104852476
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104849200-104853800 Bivalent Enhancer Fetal Muscle Trunk muscle
2 chr14:104850000-104853000 Bivalent Enhancer Placenta Placenta
3 chr14:104850200-104852600 Enhancers Fetal Muscle Leg muscle
4 chr14:104850400-104854000 Enhancers Primary B cells from peripheral blood blood
5 chr14:104850600-104856200 Enhancers Fetal Brain Female brain
6 chr14:104850800-104855400 Enhancers Brain Germinal Matrix brain
7 chr14:104850800-104859200 Weak transcription Left Ventricle heart
8 chr14:104850800-104860200 Weak transcription Gastric stomach
9 chr14:104851000-104853000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr14:104851000-104855400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr14:104851000-104855400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
12 chr14:104851000-104855600 Enhancers Fetal Brain Male brain
13 chr14:104851400-104855200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr14:104851600-104863400 Enhancers Spleen Spleen
15 chr14:104851800-104853400 Enhancers Primary B cells from cord blood blood
16 chr14:104851800-104853400 Enhancers Primary Natural Killer cells fromperipheralblood blood
17 chr14:104852000-104854200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
18 chr14:104852200-104854600 Weak transcription Primary T cells fromperipheralblood blood

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