Variant report

Variant rs73226687
Chromosome Location chr21:46428558-46428559
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46414600-46431800 Weak transcription Right Atrium heart
2 chr21:46421600-46429400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr21:46421800-46432200 Weak transcription Esophagus oesophagus
4 chr21:46426600-46432000 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr21:46426800-46429600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr21:46427200-46428800 Bivalent Enhancer HepG2 liver
7 chr21:46427400-46429000 Enhancers Dnd41 blood
8 chr21:46427400-46429800 Weak transcription Placenta Placenta
9 chr21:46427400-46430000 Weak transcription Brain Anterior Caudate brain
10 chr21:46428000-46429400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr21:46428000-46429600 Weak transcription NHEK skin
12 chr21:46428000-46430000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr21:46428400-46428800 Flanking Active TSS Hela-S3 cervix

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