Variant report

Variant rs569981494
Chromosome Location chr14:105069959-105069960
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105063800-105070000 Enhancers Fetal Brain Male brain
2 chr14:105065200-105070800 Weak transcription Right Atrium heart
3 chr14:105065400-105070000 Weak transcription Fetal Heart heart
4 chr14:105066800-105070400 Weak transcription Pancreas Pancrea
5 chr14:105068600-105070000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr14:105069000-105071800 Bivalent/Poised TSS Brain Anterior Caudate brain
7 chr14:105069000-105071800 Active TSS Brain Inferior Temporal Lobe brain
8 chr14:105069400-105070000 Active TSS Brain Dorsolateral Prefrontal Cortex brain
9 chr14:105069400-105070200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr14:105069400-105070400 Active TSS Brain Angular Gyrus brain
11 chr14:105069400-105071800 Active TSS Pancreatic Islets Pancreatic Islet
12 chr14:105069600-105070400 Bivalent/Poised TSS Brain Cingulate Gyrus brain
13 chr14:105069800-105070000 Active TSS Brain Germinal Matrix brain
14 chr14:105069800-105070000 Enhancers Fetal Brain Female brain

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