Variant report

Variant rs566241359
Chromosome Location chr6:69487737-69487738
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:69484800-69490000 Enhancers Fetal Brain Female brain
2 chr6:69485000-69490400 Enhancers Cortex derived primary cultured neurospheres brain
3 chr6:69485600-69488400 Weak transcription K562 blood
4 chr6:69486200-69489600 Enhancers Fetal Lung lung
5 chr6:69486400-69487800 Enhancers Brain Angular Gyrus brain
6 chr6:69486400-69487800 Weak transcription Fetal Brain Male brain
7 chr6:69487600-69488000 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
8 chr6:69487600-69488000 Flanking Active TSS Brain Inferior Temporal Lobe brain
9 chr6:69487600-69488200 Flanking Active TSS Brain Cingulate Gyrus brain
10 chr6:69487600-69488200 Active TSS Brain Dorsolateral Prefrontal Cortex brain
11 chr6:69487600-69488400 Flanking Active TSS Brain Anterior Caudate brain
12 chr6:69487600-69488800 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr6:69487600-69488800 Active TSS Brain Substantia Nigra brain
14 chr6:69487600-69489000 Enhancers Fetal Heart heart
15 chr6:69487600-69489200 Active TSS Brain Hippocampus Middle brain
16 chr6:69487600-69489400 Enhancers Fetal Stomach stomach
17 chr6:69487600-69491200 Enhancers Brain Germinal Matrix brain

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