Variant report

Variant rs9806007
Chromosome Location chr14:67105176-67105177
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67087000-67106800 Weak transcription Gastric stomach
2 chr14:67087200-67110000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr14:67095400-67116600 Weak transcription Brain Substantia Nigra brain
4 chr14:67095800-67112000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr14:67101400-67119600 Weak transcription Aorta Aorta
6 chr14:67101800-67109800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr14:67102000-67107800 Weak transcription Psoas Muscle Psoas
8 chr14:67102000-67110200 Weak transcription Liver Liver
9 chr14:67102000-67119400 Weak transcription Pancreas Pancrea
10 chr14:67105000-67105800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr14:67105000-67105800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr14:67105000-67106200 Enhancers HUVEC blood vessel

Quick Search:


  
Input of quick search could be:

what's new

Quick links