Variant report

Variant rs73693631
Chromosome Location chr8:67804152-67804153
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:67802400-67804200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr8:67802600-67804200 Weak transcription Brain Substantia Nigra brain
3 chr8:67802800-67804600 Weak transcription Pancreas Pancrea
4 chr8:67803000-67804200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr8:67803400-67804800 Flanking Active TSS Skeletal Muscle Male skeletal muscle
6 chr8:67803600-67804800 Flanking Active TSS Skeletal Muscle Female skeletal muscle
7 chr8:67803800-67804200 Enhancers Esophagus oesophagus
8 chr8:67803800-67804800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr8:67803800-67805000 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
10 chr8:67803800-67805000 Enhancers Right Ventricle heart
11 chr8:67804000-67804400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr8:67804000-67804400 Flanking Active TSS Left Ventricle heart
13 chr8:67804000-67804400 Weak transcription HepG2 liver
14 chr8:67804000-67804800 Enhancers Psoas Muscle Psoas

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