Variant report

Variant rs4900625
Chromosome Location chr14:104854132-104854133
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104850600-104856200 Enhancers Fetal Brain Female brain
2 chr14:104850800-104855400 Enhancers Brain Germinal Matrix brain
3 chr14:104850800-104859200 Weak transcription Left Ventricle heart
4 chr14:104850800-104860200 Weak transcription Gastric stomach
5 chr14:104851000-104855400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr14:104851000-104855400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
7 chr14:104851000-104855600 Enhancers Fetal Brain Male brain
8 chr14:104851400-104855200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr14:104851600-104863400 Enhancers Spleen Spleen
10 chr14:104852000-104854200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr14:104852200-104854600 Weak transcription Primary T cells fromperipheralblood blood
12 chr14:104853400-104857800 Weak transcription Primary B cells from cord blood blood
13 chr14:104853600-104854200 Bivalent Enhancer Adipose Nuclei Adipose
14 chr14:104853600-104854200 Enhancers Fetal Muscle Leg muscle
15 chr14:104853600-104854600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
16 chr14:104853800-104854400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
17 chr14:104853800-104855800 Weak transcription GM12878-XiMat blood
18 chr14:104853800-104862800 Enhancers Primary Natural Killer cells fromperipheralblood blood
19 chr14:104854000-104855200 Weak transcription Primary B cells from peripheral blood blood
20 chr14:104854000-104856000 Weak transcription Right Ventricle heart

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