Variant report

Variant rs58504618
Chromosome Location chr11:58598595-58598596
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58595600-58598600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr11:58596800-58604200 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr11:58597800-58599000 Weak transcription NHEK skin
4 chr11:58597800-58599400 Weak transcription HMEC breast
5 chr11:58598000-58598600 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr11:58598000-58599000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr11:58598000-58599600 Weak transcription Muscle Satellite Cultured Cells --
8 chr11:58598200-58598600 Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr11:58598200-58598600 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr11:58598200-58598600 Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr11:58598200-58598600 Enhancers Pancreas Pancrea
12 chr11:58598200-58598600 Active TSS HepG2 liver
13 chr11:58598200-58598600 Bivalent/Poised TSS Monocytes-CD14+_RO01746 blood
14 chr11:58598400-58598600 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
15 chr11:58598400-58598600 Bivalent Enhancer Sigmoid Colon Sigmoid Colon

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