Variant report

Variant rs62296943
Chromosome Location chr4:69959183-69959184
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69955600-69959400 Weak transcription HepG2 liver
2 chr4:69957400-69959600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr4:69957400-69960000 Enhancers NHEK skin
4 chr4:69957600-69959800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr4:69958000-69959200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr4:69958000-69960800 Weak transcription HUVEC blood vessel
7 chr4:69958200-69961000 Weak transcription HMEC breast
8 chr4:69958400-69961800 Weak transcription Osteobl bone
9 chr4:69958600-69959400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr4:69958600-69959400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr4:69958800-69959400 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr4:69958800-69959400 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
13 chr4:69958800-69959400 Enhancers Esophagus oesophagus
14 chr4:69958800-69959600 Enhancers Muscle Satellite Cultured Cells --
15 chr4:69958800-69959600 Enhancers NH-A brain
16 chr4:69959000-69959600 ZNF genes & repeats Fetal Intestine Small intestine

Quick Search:


  
Input of quick search could be:

what's new

Quick links