Variant report

Variant rs1990137
Chromosome Location chr7:41071830-41071831
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:41062800-41082200 Weak transcription Aorta Aorta
2 chr7:41066600-41073600 Enhancers NH-A brain
3 chr7:41069200-41074600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr7:41069400-41082000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr7:41069800-41072800 Weak transcription Osteobl bone
6 chr7:41070400-41073600 Weak transcription Pancreatic Islets Pancreatic Islet
7 chr7:41070600-41073000 Weak transcription NHDF-Ad bronchial
8 chr7:41070600-41075200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr7:41070600-41076600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr7:41070800-41072400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr7:41070800-41073000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr7:41071000-41072800 Weak transcription HMEC breast
13 chr7:41071000-41073200 Enhancers Placenta Amnion Placenta Amnion
14 chr7:41071600-41072400 Enhancers Dnd41 blood

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