Variant report

Variant nsv1022249
Chromosome Location chr8:4521513-4535022
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:4522800-4523200 Enhancers Fetal Heart heart
2 chr8:4523200-4528400 Weak transcription Fetal Heart heart
3 chr8:4527800-4529400 Enhancers Brain Germinal Matrix brain
4 chr8:4528200-4529000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr8:4528400-4529600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr8:4528400-4529800 Enhancers Cortex derived primary cultured neurospheres brain
7 chr8:4528400-4530000 Enhancers Fetal Heart heart
8 chr8:4528600-4528800 Enhancers Fetal Brain Male brain
9 chr8:4528600-4529200 Enhancers Brain Cingulate Gyrus brain
10 chr8:4529800-4532200 Weak transcription Cortex derived primary cultured neurospheres brain
11 chr8:4530000-4533200 Weak transcription Fetal Heart heart
12 chr8:4530200-4530600 Active TSS Fetal Lung lung
13 chr8:4530200-4530600 ZNF genes & repeats Pancreas Pancrea
14 chr8:4530400-4530600 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr8:4533200-4534400 Enhancers Fetal Heart heart

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