Variant report

Variant rs10164863
Chromosome Location chr2:213148179-213148180
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:213146000-213149400 Enhancers Fetal Heart heart
2 chr2:213146200-213150200 Enhancers Brain Hippocampus Middle brain
3 chr2:213146800-213148400 Enhancers Brain Cingulate Gyrus brain
4 chr2:213146800-213149000 Weak transcription Brain Angular Gyrus brain
5 chr2:213146800-213149600 Enhancers Cortex derived primary cultured neurospheres brain
6 chr2:213147200-213148200 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr2:213147200-213149000 Weak transcription Aorta Aorta
8 chr2:213147400-213148400 Enhancers Brain Anterior Caudate brain
9 chr2:213147800-213148200 Enhancers Brain Germinal Matrix brain
10 chr2:213147800-213148200 Flanking Active TSS Brain Substantia Nigra brain
11 chr2:213147800-213148800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
12 chr2:213148000-213148200 Enhancers Brain Dorsolateral Prefrontal Cortex brain
13 chr2:213148000-213149000 Weak transcription Brain Inferior Temporal Lobe brain
14 chr2:213148000-213149000 Weak transcription Psoas Muscle Psoas
15 chr2:213148000-213155000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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