Variant report

Variant rs74045702
Chromosome Location chr14:38279058-38279059
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:38266600-38279400 Weak transcription HepG2 liver
2 chr14:38276400-38279600 Weak transcription Stomach Mucosa stomach
3 chr14:38278800-38279800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
4 chr14:38278800-38280000 Enhancers H1 Cell Line embryonic stem cell
5 chr14:38278800-38280000 Enhancers HUES48 Cell Line embryonic stem cell
6 chr14:38278800-38280000 Enhancers HUES6 Cell Line embryonic stem cell
7 chr14:38278800-38280000 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr14:38278800-38280200 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr14:38278800-38280200 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr14:38279000-38279600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr14:38279000-38279800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
12 chr14:38279000-38280000 Enhancers H9 Cell Line embryonic stem cell
13 chr14:38279000-38280000 Enhancers Fetal Lung lung
14 chr14:38279000-38280200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr14:38279000-38289000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links