Variant report

Variant rs2356232
Chromosome Location chr2:171586774-171586775
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171580200-171589600 Weak transcription Fetal Intestine Small intestine
3 chr2:171580800-171590400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr2:171584800-171590600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:171585600-171586800 Strong transcription Cortex derived primary cultured neurospheres brain
6 chr2:171586000-171588200 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr2:171586200-171586800 Strong transcription Fetal Intestine Large intestine
8 chr2:171586400-171592200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

Quick Search:


  
Input of quick search could be:

what's new

Quick links