Variant report

Variant rs11999656
Chromosome Location chr9:72200566-72200567
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:72180400-72208400 Weak transcription Gastric stomach
2 chr9:72186200-72200800 Weak transcription HSMMtube muscle
3 chr9:72187400-72204800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr9:72193200-72204400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
5 chr9:72195400-72200600 Weak transcription Sigmoid Colon Sigmoid Colon
6 chr9:72195800-72208200 Weak transcription Fetal Lung lung
7 chr9:72196000-72204800 Weak transcription Fetal Brain Male brain
8 chr9:72196200-72204800 Weak transcription Brain Inferior Temporal Lobe brain
9 chr9:72196400-72201000 Enhancers HUVEC blood vessel
10 chr9:72197200-72201000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr9:72198600-72200800 Enhancers NHDF-Ad bronchial
12 chr9:72199000-72204200 Weak transcription Brain Germinal Matrix brain
13 chr9:72199200-72200600 Enhancers NH-A brain
14 chr9:72199400-72200600 Enhancers Osteobl bone
15 chr9:72199600-72204200 Weak transcription Cortex derived primary cultured neurospheres brain
16 chr9:72200000-72200600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
17 chr9:72200200-72201200 Enhancers Fetal Heart heart
18 chr9:72200400-72200600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
19 chr9:72200400-72201000 Enhancers Skeletal Muscle Female skeletal muscle

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