Variant report

Variant rs553645815
Chromosome Location chr2:87034175-87034176
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:87032800-87034400 Weak transcription Right Atrium heart
2 chr2:87033200-87034200 Enhancers Primary Natural Killer cells fromperipheralblood blood
3 chr2:87033200-87034600 Flanking Active TSS Fetal Thymus thymus
4 chr2:87033200-87034800 Flanking Active TSS Primary T killer naive cells fromperipheralblood blood
5 chr2:87033200-87035000 Active TSS Primary T cells from cord blood blood
6 chr2:87033400-87034200 Bivalent Enhancer Placenta Placenta
7 chr2:87033600-87034400 Enhancers Brain Angular Gyrus brain
8 chr2:87033600-87034600 Weak transcription Esophagus oesophagus
9 chr2:87033600-87034600 Enhancers Spleen Spleen
10 chr2:87033800-87034400 Weak transcription Primary T killer memory cells from peripheral blood blood
11 chr2:87033800-87034600 Active TSS Primary mononuclear cells fromperipheralblood Blood
12 chr2:87034000-87034200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr2:87034000-87034200 Flanking Active TSS Fetal Brain Female brain
14 chr2:87034000-87034200 Bivalent Enhancer HepG2 liver
15 chr2:87034000-87034400 Weak transcription Fetal Brain Male brain
16 chr2:87034000-87034400 Enhancers Fetal Heart heart
17 chr2:87034000-87034600 Active TSS Primary T helper naive cells from peripheral blood blood
18 chr2:87034000-87037000 Active TSS Thymus Thymus
19 chr2:87034000-87037400 Flanking Bivalent TSS/Enh Primary T cells fromperipheralblood blood

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