Variant report

Variant rs11884652
Chromosome Location chr2:210413185-210413186
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210410400-210420000 Weak transcription Fetal Brain Male brain
2 chr2:210410600-210430800 Weak transcription Fetal Brain Female brain
3 chr2:210411200-210413600 Enhancers Cortex derived primary cultured neurospheres brain
4 chr2:210411200-210413600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr2:210412200-210413200 Enhancers Brain Germinal Matrix brain
6 chr2:210412600-210413200 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:210413000-210413200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr2:210413000-210414000 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr2:210413000-210414600 Weak transcription Pancreatic Islets Pancreatic Islet

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