Variant report

Variant rs7874239
Chromosome Location chr9:140968222-140968223
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140933000-140976400 Weak transcription Right Atrium heart
2 chr9:140954200-140979000 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr9:140956800-140975200 Weak transcription Brain Angular Gyrus brain
4 chr9:140960800-140968400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
5 chr9:140960800-140970600 Weak transcription Fetal Brain Female brain
6 chr9:140963600-140978600 Weak transcription Fetal Brain Male brain
7 chr9:140963800-140970000 Weak transcription Brain Germinal Matrix brain
8 chr9:140966800-140968600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:140967000-140968400 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr9:140967200-140968600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
11 chr9:140967200-140968600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr9:140967200-140968600 Enhancers Brain Anterior Caudate brain
13 chr9:140967600-140968400 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr9:140968000-140968600 Enhancers Brain Cingulate Gyrus brain
15 chr9:140968000-140972600 Weak transcription HUES48 Cell Line embryonic stem cell
16 chr9:140968000-140977200 Weak transcription iPS-15b Cell Line embryonic stem cell
17 chr9:140968200-140977400 Weak transcription HUES6 Cell Line embryonic stem cell

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