Variant report

Variant rs10165706
Chromosome Location chr2:134389122-134389123
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:134368000-134389800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:134382400-134389600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr2:134382400-134389600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr2:134382600-134389600 Weak transcription NHEK skin
5 chr2:134385200-134390600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr2:134386000-134390600 Weak transcription Brain Angular Gyrus brain
7 chr2:134386800-134392000 ZNF genes & repeats H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr2:134388400-134391600 Weak transcription Right Atrium heart
9 chr2:134388800-134389400 Weak transcription Brain Substantia Nigra brain
10 chr2:134389000-134389600 Weak transcription Brain Hippocampus Middle brain

Quick Search:


  
Input of quick search could be:

what's new

Quick links