Variant report

Variant rs72747008
Chromosome Location chr9:97467957-97467958
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:97465800-97469600 Enhancers Fetal Lung lung
2 chr9:97465800-97469600 Enhancers Fetal Stomach stomach
3 chr9:97466000-97468400 Weak transcription Small Intestine intestine
4 chr9:97466600-97469200 Weak transcription Liver Liver
5 chr9:97466600-97469200 Weak transcription Fetal Intestine Large intestine
6 chr9:97466600-97469800 Enhancers HepG2 liver
7 chr9:97467200-97469000 Enhancers Brain Germinal Matrix brain
8 chr9:97467200-97469000 Enhancers Placenta Placenta
9 chr9:97467400-97468000 Active TSS Brain Angular Gyrus brain
10 chr9:97467400-97468200 Enhancers Cortex derived primary cultured neurospheres brain
11 chr9:97467400-97469800 Enhancers Fetal Intestine Small intestine
12 chr9:97467600-97468000 Active TSS Brain Anterior Caudate brain
13 chr9:97467600-97468000 Active TSS Brain Hippocampus Middle brain
14 chr9:97467600-97468000 Active TSS Brain Inferior Temporal Lobe brain
15 chr9:97467600-97468000 Active TSS Brain Substantia Nigra brain
16 chr9:97467800-97468000 Flanking Active TSS Stomach Smooth Muscle stomach
17 chr9:97467800-97468400 Enhancers Colon Smooth Muscle Colon
18 chr9:97467800-97468400 Enhancers Fetal Brain Female brain
19 chr9:97467800-97468600 Enhancers Fetal Kidney kidney

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