Variant report

Variant rs56199155
Chromosome Location chr14:104820232-104820233
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104816800-104820400 Weak transcription Fetal Brain Male brain
2 chr14:104817600-104820400 Weak transcription Fetal Lung lung
3 chr14:104819600-104820400 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr14:104819600-104820400 Enhancers Spleen Spleen
5 chr14:104819600-104820800 Bivalent Enhancer Right Ventricle heart
6 chr14:104819800-104820400 ZNF genes & repeats Lung lung
7 chr14:104819800-104821000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr14:104819800-104822000 Bivalent Enhancer Fetal Stomach stomach
9 chr14:104820000-104823400 Enhancers Brain Germinal Matrix brain
10 chr14:104820000-104823600 Enhancers Fetal Muscle Leg muscle
11 chr14:104820000-104824200 Bivalent Enhancer Fetal Muscle Trunk muscle
12 chr14:104820200-104821000 Bivalent Enhancer Adipose Nuclei Adipose
13 chr14:104820200-104821000 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
14 chr14:104820200-104822400 Enhancers Left Ventricle heart
15 chr14:104820200-104823000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland

Quick Search:


  
Input of quick search could be:

what's new

Quick links