Variant report

Variant rs3812940
Chromosome Location chr15:34788566-34788567
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:34787000-34788600 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr15:34787400-34788800 Bivalent Enhancer Esophagus oesophagus
3 chr15:34787600-34788600 Bivalent Enhancer Fetal Muscle Leg muscle
4 chr15:34787800-34789200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
5 chr15:34788000-34788800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr15:34788000-34790800 Weak transcription Pancreas Pancrea
7 chr15:34788400-34788600 Bivalent/Poised TSS Foreskin Melanocyte Primary Cells skin01 Skin
8 chr15:34788400-34788600 Bivalent Enhancer Fetal Lung lung
9 chr15:34788400-34788600 Flanking Bivalent TSS/Enh Fetal Muscle Trunk muscle
10 chr15:34788400-34788600 Bivalent/Poised TSS Lung lung
11 chr15:34788400-34788800 Flanking Bivalent TSS/Enh Adipose Nuclei Adipose
12 chr15:34788400-34789200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr15:34788400-34789200 Active TSS Right Atrium heart
14 chr15:34788400-34789400 Bivalent/Poised TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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