Variant report

Variant rs1921756
Chromosome Location chr7:40880591-40880592
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:40867600-40882600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr7:40874000-40883400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr7:40880000-40881600 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:40880000-40883200 Weak transcription NH-A brain
5 chr7:40880000-40883200 Weak transcription Osteobl bone
6 chr7:40880200-40881200 Weak transcription NHEK skin
7 chr7:40880200-40905400 Weak transcription HSMMtube muscle
8 chr7:40880400-40880600 Weak transcription HMEC breast
9 chr7:40880400-40889600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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