Variant report

Variant rs568836124
Chromosome Location chr15:30259789-30259790
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:30232600-30260400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr15:30255600-30260000 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr15:30257200-30260400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr15:30259000-30259800 Enhancers Brain Substantia Nigra brain
5 chr15:30259200-30262200 Active TSS Brain Anterior Caudate brain
6 chr15:30259400-30259800 Flanking Active TSS Brain Cingulate Gyrus brain
7 chr15:30259600-30259800 Flanking Active TSS Brain Hippocampus Middle brain
8 chr15:30259600-30259800 Flanking Active TSS Brain Inferior Temporal Lobe brain
9 chr15:30259600-30259800 Flanking Active TSS Brain Dorsolateral Prefrontal Cortex brain
10 chr15:30259600-30259800 Bivalent Enhancer Fetal Brain Male brain
11 chr15:30259600-30260400 Enhancers Liver Liver
12 chr15:30259600-30262000 Active TSS Brain Angular Gyrus brain

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