Variant report

Variant rs74089076
Chromosome Location chr14:105120503-105120504
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105116800-105120600 Weak transcription Brain Angular Gyrus brain
2 chr14:105116800-105125800 Weak transcription ES-WA7 Cell Line embryonic stem cell
3 chr14:105116800-105125800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr14:105116800-105131600 Weak transcription Right Atrium heart
5 chr14:105117200-105123200 Weak transcription Brain Hippocampus Middle brain
6 chr14:105117800-105120800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
7 chr14:105118200-105121000 Enhancers Liver Liver
8 chr14:105120000-105120800 Enhancers Pancreas Pancrea
9 chr14:105120000-105121000 Enhancers HepG2 liver
10 chr14:105120200-105120600 Enhancers Spleen Spleen
11 chr14:105120200-105123000 Enhancers Primary B cells from peripheral blood blood
12 chr14:105120400-105120600 Bivalent Enhancer Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr14:105120400-105120800 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr14:105120400-105122800 Weak transcription Primary T cells from cord blood blood

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