Variant report

Variant rs529703376
Chromosome Location chr14:105011279-105011280
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105008000-105011600 Enhancers Brain Germinal Matrix brain
2 chr14:105008000-105011600 Enhancers Fetal Brain Female brain
3 chr14:105008000-105016600 Enhancers Fetal Brain Male brain
4 chr14:105008600-105012000 Enhancers Cortex derived primary cultured neurospheres brain
5 chr14:105009600-105012400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr14:105009800-105014600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr14:105011000-105011600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr14:105011000-105011600 Enhancers Brain Substantia Nigra brain
9 chr14:105011200-105011400 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
10 chr14:105011200-105011400 Bivalent/Poised TSS Fetal Lung lung
11 chr14:105011200-105011600 Bivalent Enhancer Brain Cingulate Gyrus brain
12 chr14:105011200-105011800 Bivalent Enhancer Brain Anterior Caudate brain
13 chr14:105011200-105012000 Enhancers Brain Inferior Temporal Lobe brain

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