Variant report

Variant rs527842807
Chromosome Location chr2:210635969-210635970
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210632600-210636200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr2:210635600-210637200 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
3 chr2:210635800-210636000 Enhancers Cortex derived primary cultured neurospheres brain
4 chr2:210635800-210636000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
5 chr2:210635800-210636000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr2:210635800-210636000 Enhancers Brain Anterior Caudate brain
7 chr2:210635800-210636000 Enhancers Brain Inferior Temporal Lobe brain
8 chr2:210635800-210636000 Enhancers Brain Dorsolateral Prefrontal Cortex brain
9 chr2:210635800-210636000 Enhancers Fetal Brain Male brain
10 chr2:210635800-210637200 Active TSS H9 Derived Neuron Cultured Cells ES cell derived

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