Variant report

Variant rs2405391
Chromosome Location chr20:23568790-23568791
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:23567200-23569200 Weak transcription Fetal Thymus thymus
2 chr20:23567600-23569000 Weak transcription Stomach Mucosa stomach
3 chr20:23568000-23569200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr20:23568000-23569400 Weak transcription NHEK skin
5 chr20:23568200-23569200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr20:23568200-23569200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr20:23568200-23569600 Weak transcription HMEC breast
8 chr20:23568400-23569400 Weak transcription Fetal Intestine Small intestine
9 chr20:23568400-23570000 Enhancers HepG2 liver
10 chr20:23568600-23569600 Weak transcription Placenta Placenta

Quick Search:


  
Input of quick search could be:

what's new

Quick links