Variant report

Variant rs4779897
Chromosome Location chr15:31879058-31879059
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:31862400-31897000 Weak transcription Gastric stomach
2 chr15:31868200-31880800 Weak transcription H9 Cell Line embryonic stem cell
3 chr15:31872200-31886600 Weak transcription Brain Anterior Caudate brain
4 chr15:31875400-31883800 Weak transcription Brain Substantia Nigra brain
5 chr15:31875600-31882400 Weak transcription Brain Hippocampus Middle brain
6 chr15:31876600-31879200 Enhancers Placenta Amnion Placenta Amnion
7 chr15:31877400-31886800 Weak transcription Brain Angular Gyrus brain
8 chr15:31877800-31900800 Weak transcription Pancreas Pancrea
9 chr15:31878400-31879400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr15:31878800-31879400 Enhancers Brain Dorsolateral Prefrontal Cortex brain
11 chr15:31878800-31880000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr15:31879000-31879200 Bivalent Enhancer NHEK skin
13 chr15:31879000-31879600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr15:31879000-31886600 Weak transcription Brain Cingulate Gyrus brain

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