Variant report

Variant rs4943036
Chromosome Location chr13:52449879-52449880
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:52433800-52479400 Weak transcription HepG2 liver
2 chr13:52438200-52455400 Weak transcription Fetal Intestine Small intestine
3 chr13:52446200-52457000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr13:52448000-52450000 Enhancers Cortex derived primary cultured neurospheres brain
5 chr13:52448200-52457000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr13:52449200-52450000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
7 chr13:52449800-52450400 Enhancers Fetal Thymus thymus

Quick Search:


  
Input of quick search could be:

what's new

Quick links