Variant report

Variant rs78354537
Chromosome Location chr14:105012865-105012866
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105008000-105016600 Enhancers Fetal Brain Male brain
2 chr14:105009800-105014600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr14:105011600-105013000 Bivalent Enhancer Fetal Muscle Leg muscle
4 chr14:105011600-105013800 Bivalent Enhancer Fetal Muscle Trunk muscle
5 chr14:105011800-105013000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
6 chr14:105011800-105013400 Bivalent Enhancer Fetal Stomach stomach
7 chr14:105012200-105013000 Flanking Active TSS Brain Germinal Matrix brain
8 chr14:105012400-105013000 Enhancers Brain Angular Gyrus brain
9 chr14:105012400-105013000 Enhancers Brain Anterior Caudate brain
10 chr14:105012400-105013000 Bivalent Enhancer Brain Hippocampus Middle brain
11 chr14:105012600-105013600 Enhancers Cortex derived primary cultured neurospheres brain
12 chr14:105012600-105014800 Weak transcription Spleen Spleen
13 chr14:105012600-105015400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
14 chr14:105012600-105016000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr14:105012800-105013400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr14:105012800-105014400 Enhancers Fetal Brain Female brain

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