Variant report

Variant rs4862638
Chromosome Location chr4:187029807-187029808
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:187027800-187031000 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr4:187029000-187030000 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr4:187029000-187030000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
4 chr4:187029000-187030000 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr4:187029000-187030000 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr4:187029000-187038600 Weak transcription Pancreas Pancrea
7 chr4:187029200-187030000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr4:187029200-187030000 Enhancers Cortex derived primary cultured neurospheres brain
9 chr4:187029200-187030800 Weak transcription Pancreatic Islets Pancreatic Islet
10 chr4:187029800-187030000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
11 chr4:187029800-187043400 Weak transcription Lung lung

Quick Search:


  
Input of quick search could be:

what's new

Quick links