Variant report

Variant rs34123628
Chromosome Location chr6:150579419-150579420
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:150574800-150590800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr6:150576400-150579600 Weak transcription K562 blood
3 chr6:150576400-150580400 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr6:150577400-150585200 Weak transcription Right Ventricle heart
5 chr6:150577400-150585400 Weak transcription Left Ventricle heart
6 chr6:150577400-150588200 Weak transcription Psoas Muscle Psoas
7 chr6:150577600-150580400 Weak transcription Skeletal Muscle Male skeletal muscle
8 chr6:150577800-150580000 Enhancers HMEC breast
9 chr6:150578000-150589000 Weak transcription Skeletal Muscle Female skeletal muscle
10 chr6:150578200-150580600 Weak transcription Fetal Heart heart
11 chr6:150578400-150588000 Weak transcription NH-A brain
12 chr6:150579200-150587600 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr6:150579400-150579600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr6:150579400-150584200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr6:150579400-150587200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr6:150579400-150587200 Weak transcription NHEK skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links