Variant report

Variant rs4886916
Chromosome Location chr15:78090405-78090406
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:78073800-78099200 Weak transcription Right Atrium heart
2 chr15:78074400-78100800 Weak transcription Fetal Intestine Small intestine
3 chr15:78079600-78092400 Weak transcription Brain Inferior Temporal Lobe brain
4 chr15:78079600-78096400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
5 chr15:78080400-78095000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr15:78087600-78090800 Enhancers Dnd41 blood
7 chr15:78088200-78090800 Weak transcription Fetal Brain Female brain
8 chr15:78088200-78092400 Enhancers Fetal Thymus thymus
9 chr15:78089600-78091200 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr15:78089800-78090600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr15:78090000-78091200 Enhancers Cortex derived primary cultured neurospheres brain
12 chr15:78090200-78091800 Weak transcription Fetal Muscle Leg muscle
13 chr15:78090400-78090800 Enhancers Pancreas Pancrea
14 chr15:78090400-78091000 Enhancers Brain Angular Gyrus brain
15 chr15:78090400-78091200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain

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