Variant report

Variant rs2097018
Chromosome Location chr11:58597800-58597801
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr11:58596600-58597800 Enhancers HMEC breast
3 chr11:58596600-58597800 Enhancers NHEK skin
4 chr11:58596600-58598000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr11:58596600-58598000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr11:58596600-58598000 Enhancers Muscle Satellite Cultured Cells --
7 chr11:58596800-58604200 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr11:58597200-58598000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr11:58597200-58598200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr11:58597600-58597800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr11:58597600-58597800 Enhancers Hela-S3 cervix
12 chr11:58597600-58597800 Enhancers Osteobl bone
13 chr11:58597600-58598000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr11:58597600-58598000 Enhancers NHDF-Ad bronchial
15 chr11:58597600-58598200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr11:58597800-58598200 Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
17 chr11:58597800-58599000 Weak transcription NHEK skin
18 chr11:58597800-58599400 Weak transcription HMEC breast

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