Variant report

Variant rs17490375
Chromosome Location chr11:58426485-58426486
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58423400-58427000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr11:58425600-58428000 Enhancers HMEC breast
3 chr11:58425800-58428000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr11:58426000-58427600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr11:58426000-58427600 Enhancers NHEK skin
6 chr11:58426000-58427800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr11:58426000-58428200 Enhancers Stomach Mucosa stomach
8 chr11:58426000-58429000 Enhancers Fetal Intestine Large intestine
9 chr11:58426200-58427400 Weak transcription Esophagus oesophagus
10 chr11:58426200-58428200 Enhancers Fetal Intestine Small intestine
11 chr11:58426400-58428000 Enhancers Hela-S3 cervix

Quick Search:


  
Input of quick search could be:

what's new

Quick links