Variant report

Variant rs10989443
Chromosome Location chr9:103992600-103992601
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:103987400-103995200 Weak transcription Fetal Brain Female brain
2 chr9:103989600-103992600 Weak transcription Brain Angular Gyrus brain
3 chr9:103989600-103993400 Weak transcription HepG2 liver
4 chr9:103991200-103994400 Enhancers Cortex derived primary cultured neurospheres brain
5 chr9:103991400-103994800 Enhancers Brain Cingulate Gyrus brain
6 chr9:103992000-103992800 Enhancers Fetal Brain Male brain
7 chr9:103992000-103993000 Enhancers H9 Cell Line embryonic stem cell
8 chr9:103992000-103994200 Enhancers Brain Substantia Nigra brain
9 chr9:103992000-103994600 Enhancers Brain Anterior Caudate brain
10 chr9:103992000-103994800 Enhancers HUES64 Cell Line embryonic stem cell
11 chr9:103992000-103995400 Enhancers Liver Liver
12 chr9:103992400-103992800 Flanking Active TSS Brain Hippocampus Middle brain
13 chr9:103992400-103993600 Enhancers Brain Inferior Temporal Lobe brain
14 chr9:103992400-103994600 Enhancers HUES48 Cell Line embryonic stem cell
15 chr9:103992400-103997400 Weak transcription Pancreatic Islets Pancreatic Islet
16 chr9:103992600-103993000 Enhancers ES-I3 Cell Line embryonic stem cell
17 chr9:103992600-103993000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
18 chr9:103992600-103993000 Enhancers Brain Angular Gyrus brain
19 chr9:103992600-103993800 Enhancers H1 Cell Line embryonic stem cell

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