Variant report

Variant rs9978078
Chromosome Location chr21:47176154-47176155
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47166200-47176800 Weak transcription Dnd41 blood
2 chr21:47166200-47194400 Weak transcription Primary neutrophils fromperipheralblood blood
3 chr21:47167800-47176200 Weak transcription NH-A brain
4 chr21:47168600-47187000 Weak transcription NHDF-Ad bronchial
5 chr21:47168800-47183000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr21:47170000-47179800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr21:47170200-47188800 Weak transcription Spleen Spleen
8 chr21:47170800-47188200 Weak transcription Right Atrium heart
9 chr21:47171800-47179400 Weak transcription Fetal Thymus thymus
10 chr21:47171800-47180000 Weak transcription Thymus Thymus
11 chr21:47171800-47186600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr21:47175400-47176800 Enhancers HepG2 liver
13 chr21:47175600-47186000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr21:47176000-47176800 ZNF genes & repeats Primary T cells from cord blood blood
15 chr21:47176000-47177200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --

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