Variant report

Variant rs10169878
Chromosome Location chr2:213195254-213195255
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:213168800-213197200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr2:213194200-213195800 Enhancers Fetal Heart heart
3 chr2:213194400-213195400 Enhancers Brain Inferior Temporal Lobe brain
4 chr2:213194600-213195400 Enhancers Brain Cingulate Gyrus brain
5 chr2:213194800-213195400 Enhancers Right Ventricle heart
6 chr2:213194800-213195800 Active TSS Aorta Aorta
7 chr2:213195000-213195400 Flanking Active TSS Brain Angular Gyrus brain
8 chr2:213195000-213195600 Enhancers Brain Anterior Caudate brain
9 chr2:213195000-213195600 Enhancers Brain Substantia Nigra brain
10 chr2:213195200-213195600 Enhancers Brain Hippocampus Middle brain
11 chr2:213195200-213195600 Enhancers Skeletal Muscle Female skeletal muscle

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