Variant report

Variant rs367606175
Chromosome Location chr3:21985829-21985830
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:21982000-21987200 Weak transcription Fetal Lung lung
2 chr3:21984600-21986000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr3:21984600-21996000 Weak transcription Muscle Satellite Cultured Cells --
4 chr3:21984800-21988400 Weak transcription NHLF lung
5 chr3:21985200-21986000 Active TSS Fetal Stomach stomach
6 chr3:21985200-21987400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr3:21985400-21986200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr3:21985600-21986000 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
9 chr3:21985600-21986000 Active TSS Stomach Smooth Muscle stomach
10 chr3:21985600-21986400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr3:21985800-21986200 Flanking Active TSS Cortex derived primary cultured neurospheres brain
12 chr3:21985800-21986200 Enhancers Fetal Heart heart
13 chr3:21985800-21986200 Flanking Active TSS NHDF-Ad bronchial
14 chr3:21985800-21986400 Enhancers Fetal Kidney kidney
15 chr3:21985800-21986800 Weak transcription Pancreatic Islets Pancreatic Islet

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