Variant report

Variant rs7029565
Chromosome Location chr9:139878317-139878318
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139873600-139886200 Weak transcription Pancreas Pancrea
2 chr9:139873800-139879600 Weak transcription H9 Cell Line embryonic stem cell
3 chr9:139875000-139878400 Flanking Active TSS Hela-S3 cervix
4 chr9:139875600-139879000 Enhancers Brain Hippocampus Middle brain
5 chr9:139876600-139879400 Enhancers Right Ventricle heart
6 chr9:139876800-139879400 Enhancers Brain Dorsolateral Prefrontal Cortex brain
7 chr9:139876800-139880800 Enhancers Brain Substantia Nigra brain
8 chr9:139877000-139878600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:139877000-139879600 Enhancers Brain Anterior Caudate brain
10 chr9:139877000-139879600 Enhancers Brain Inferior Temporal Lobe brain
11 chr9:139877600-139878800 Weak transcription Left Ventricle heart
12 chr9:139877600-139879200 Weak transcription Placenta Placenta
13 chr9:139878000-139879200 Enhancers Brain Cingulate Gyrus brain
14 chr9:139878200-139878400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
15 chr9:139878200-139878400 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
16 chr9:139878200-139879800 Enhancers Brain Angular Gyrus brain

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