Variant report

Variant rs35112486
Chromosome Location chr9:73149220-73149221
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:73141000-73149800 Weak transcription NHLF lung
2 chr9:73145400-73151000 Weak transcription Adipose Nuclei Adipose
3 chr9:73145400-73154000 Weak transcription Left Ventricle heart
4 chr9:73146800-73154000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr9:73148400-73150400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr9:73148400-73151400 Enhancers Osteobl bone
7 chr9:73148800-73149600 Flanking Active TSS HUVEC blood vessel
8 chr9:73148800-73150000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr9:73148800-73151000 Enhancers Fetal Heart heart
10 chr9:73149000-73149800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr9:73149000-73150000 Enhancers Muscle Satellite Cultured Cells --
12 chr9:73149200-73153800 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr9:73149200-73153800 Weak transcription Brain Angular Gyrus brain
14 chr9:73149200-73154200 Weak transcription HUES6 Cell Line embryonic stem cell
15 chr9:73149200-73156000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
16 chr9:73149200-73162200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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