Variant report

Variant rs11137362
Chromosome Location chr9:140965873-140965874
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140933000-140976400 Weak transcription Right Atrium heart
2 chr9:140954000-140968000 Weak transcription Brain Cingulate Gyrus brain
3 chr9:140954200-140979000 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr9:140956800-140975200 Weak transcription Brain Angular Gyrus brain
5 chr9:140958000-140967200 Weak transcription Brain Anterior Caudate brain
6 chr9:140960800-140966600 Weak transcription Brain Inferior Temporal Lobe brain
7 chr9:140960800-140968400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
8 chr9:140960800-140970600 Weak transcription Fetal Brain Female brain
9 chr9:140962400-140966000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr9:140963600-140978600 Weak transcription Fetal Brain Male brain
11 chr9:140963800-140970000 Weak transcription Brain Germinal Matrix brain
12 chr9:140964600-140967200 Weak transcription HUES48 Cell Line embryonic stem cell
13 chr9:140964800-140967600 Weak transcription HUES64 Cell Line embryonic stem cell
14 chr9:140965200-140967000 Weak transcription HUES6 Cell Line embryonic stem cell
15 chr9:140965200-140967000 Weak transcription iPS-18 Cell Line embryonic stem cell
16 chr9:140965200-140967200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
17 chr9:140965400-140967200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
18 chr9:140965400-140967600 Weak transcription iPS-15b Cell Line embryonic stem cell
19 chr9:140965400-140967800 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin

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