Variant report

Variant rs6495676
Chromosome Location chr15:34789133-34789134
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:34787800-34789200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
2 chr15:34788000-34790800 Weak transcription Pancreas Pancrea
3 chr15:34788400-34789200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr15:34788400-34789200 Active TSS Right Atrium heart
5 chr15:34788400-34789400 Bivalent/Poised TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr15:34788800-34789200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
7 chr15:34788800-34789200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
8 chr15:34788800-34789200 Bivalent Enhancer Fetal Muscle Leg muscle
9 chr15:34789000-34789200 Active TSS Adipose Nuclei Adipose
10 chr15:34789000-34789200 Bivalent/Poised TSS Brain Hippocampus Middle brain
11 chr15:34789000-34789200 Flanking Bivalent TSS/Enh Fetal Muscle Trunk muscle
12 chr15:34789000-34789200 Bivalent Enhancer Fetal Stomach stomach
13 chr15:34789000-34789200 Flanking Bivalent TSS/Enh Psoas Muscle Psoas
14 chr15:34789000-34789800 Bivalent Enhancer Fetal Brain Male brain

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