Variant report

Variant rs13386656
Chromosome Location chr2:210431423-210431424
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210428400-210431800 Weak transcription Aorta Aorta
2 chr2:210430400-210432200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
3 chr2:210430600-210431600 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
4 chr2:210430600-210431600 Flanking Active TSS Pancreatic Islets Pancreatic Islet
5 chr2:210430800-210431600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr2:210430800-210431800 Enhancers Fetal Brain Female brain
7 chr2:210431200-210432200 Enhancers Cortex derived primary cultured neurospheres brain

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