Variant report

Variant rs28756262
Chromosome Location chr13:52934247-52934248
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:52931000-52935400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr13:52931200-52935200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr13:52931400-52935200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr13:52931400-52935200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr13:52931400-52935400 Weak transcription HMEC breast
6 chr13:52931400-52935400 Weak transcription NHEK skin
7 chr13:52931400-52935600 Weak transcription Osteobl bone
8 chr13:52931400-52937200 Weak transcription NH-A brain
9 chr13:52932800-52934800 Enhancers Fetal Muscle Leg muscle
10 chr13:52933200-52934600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr13:52933400-52934400 Enhancers Cortex derived primary cultured neurospheres brain
12 chr13:52933800-52934400 Enhancers NHDF-Ad bronchial
13 chr13:52934000-52951800 Weak transcription Fetal Intestine Small intestine
14 chr13:52934200-52934400 Enhancers Fetal Lung lung

Quick Search:


  
Input of quick search could be:

what's new

Quick links