Variant report

Variant rs10870198
Chromosome Location chr9:140042320-140042321
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140033600-140054400 Weak transcription Right Atrium heart
2 chr9:140041200-140042400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
3 chr9:140041600-140042400 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
4 chr9:140041800-140042800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
5 chr9:140041800-140047000 Weak transcription Spleen Spleen
6 chr9:140042000-140043000 Weak transcription Brain Anterior Caudate brain
7 chr9:140042000-140043200 Weak transcription Brain Inferior Temporal Lobe brain
8 chr9:140042000-140043400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
9 chr9:140042000-140047200 Weak transcription Pancreas Pancrea
10 chr9:140042000-140047400 Weak transcription H9 Cell Line embryonic stem cell
11 chr9:140042000-140047400 Weak transcription Gastric stomach
12 chr9:140042200-140042400 Strong transcription Fetal Brain Female brain
13 chr9:140042200-140043200 Weak transcription Brain Angular Gyrus brain
14 chr9:140042200-140043800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr9:140042200-140047200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr9:140042200-140049400 Weak transcription Brain Cingulate Gyrus brain

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