Variant report

Variant rs1425052
Chromosome Location chr8:120213015-120213016
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:120212600-120213400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:120212600-120213400 Enhancers Placenta Placenta
3 chr8:120212600-120213600 Enhancers NHEK skin
4 chr8:120212600-120213800 Enhancers Adipose Nuclei Adipose
5 chr8:120212800-120213400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr8:120212800-120213400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr8:120212800-120213600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr8:120212800-120213600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr8:120212800-120213600 Enhancers HMEC breast
10 chr8:120212800-120218600 Weak transcription Esophagus oesophagus
11 chr8:120213000-120213400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr8:120213000-120213400 Enhancers Fetal Intestine Large intestine
13 chr8:120213000-120213400 Flanking Active TSS Hela-S3 cervix
14 chr8:120213000-120213400 Bivalent Enhancer NHDF-Ad bronchial
15 chr8:120213000-120215200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived

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