Variant report

Variant rs12685549
Chromosome Location chr9:18865803-18865804
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18858800-18876600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr9:18862400-18866800 Weak transcription Right Ventricle heart
3 chr9:18862600-18866200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr9:18862800-18870000 Weak transcription Duodenum Smooth Muscle Duodenum
5 chr9:18863000-18871200 Strong transcription HSMM muscle
6 chr9:18863600-18866000 Enhancers NHDF-Ad bronchial
7 chr9:18863800-18881800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr9:18864400-18868200 Weak transcription Muscle Satellite Cultured Cells --
9 chr9:18864400-18868800 Weak transcription Aorta Aorta
10 chr9:18864400-18883000 Weak transcription NH-A brain
11 chr9:18864800-18869000 Weak transcription Fetal Stomach stomach
12 chr9:18865000-18868800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr9:18865000-18869200 Weak transcription Fetal Muscle Leg muscle
14 chr9:18865400-18866000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr9:18865600-18866000 Enhancers Fetal Brain Male brain
16 chr9:18865600-18866400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr9:18865600-18867200 Enhancers Osteobl bone

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