Variant report

Variant rs72821406
Chromosome Location chr2:95987575-95987576
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:95980400-95991000 Weak transcription Fetal Brain Female brain
2 chr2:95983000-95996000 Weak transcription Brain Substantia Nigra brain
3 chr2:95983000-95996400 Weak transcription Brain Angular Gyrus brain
4 chr2:95983000-95996400 Weak transcription Brain Hippocampus Middle brain
5 chr2:95983800-95989200 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr2:95985400-95988200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr2:95985600-95989000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr2:95986000-95988200 Weak transcription Esophagus oesophagus
9 chr2:95986400-95988400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr2:95987200-95988600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
11 chr2:95987400-95987800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr2:95987400-95987800 Flanking Active TSS NHDF-Ad bronchial
13 chr2:95987400-95996000 Weak transcription Placenta Amnion Placenta Amnion

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