Variant report

Variant rs79121305
Chromosome Location chr10:42737226-42737227
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:42732400-42742600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr10:42737000-42737400 Enhancers Primary hematopoietic stem cells blood
3 chr10:42737000-42737400 Active TSS HMEC breast
4 chr10:42737000-42737400 ZNF genes & repeats HSMMtube muscle
5 chr10:42737000-42737400 Bivalent Enhancer NHEK skin
6 chr10:42737000-42737600 Enhancers Osteobl bone
7 chr10:42737000-42738400 ZNF genes & repeats IMR90 fetal lung fibroblasts Cell Line lung
8 chr10:42737000-42738400 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain
9 chr10:42737200-42737400 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
10 chr10:42737200-42737400 ZNF genes & repeats Primary hematopoietic stem cells short term culture blood
11 chr10:42737200-42737400 Enhancers Brain Substantia Nigra brain
12 chr10:42737200-42737400 Enhancers Pancreatic Islets Pancreatic Islet
13 chr10:42737200-42737400 Flanking Active TSS HSMM muscle
14 chr10:42737200-42737400 ZNF genes & repeats NH-A brain
15 chr10:42737200-42737600 ZNF genes & repeats H1 Cell Line embryonic stem cell
16 chr10:42737200-42738200 Bivalent/Poised TSS Breast Myoepithelial Primary Cells Breast

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