Variant report

Variant rs75930507
Chromosome Location chr13:52919357-52919358
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:52917600-52920400 Enhancers Osteobl bone
2 chr13:52917800-52920400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr13:52917800-52922000 Weak transcription A549 lung
4 chr13:52918200-52920400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr13:52918200-52920600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr13:52918400-52920600 Enhancers Muscle Satellite Cultured Cells --
7 chr13:52918600-52919400 Weak transcription NHDF-Ad bronchial
8 chr13:52918600-52919600 Enhancers NHLF lung
9 chr13:52918600-52919800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr13:52918600-52920000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr13:52918800-52920400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr13:52918800-52920800 Enhancers HSMMtube muscle
13 chr13:52918800-52924000 Enhancers HSMM muscle
14 chr13:52918800-52924400 Enhancers HMEC breast
15 chr13:52919000-52920400 Enhancers HUVEC blood vessel
16 chr13:52919200-52919600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr13:52919200-52920000 Flanking Active TSS NHEK skin
18 chr13:52919200-52920400 Enhancers NH-A brain
19 chr13:52919200-52921800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
20 chr13:52919200-52922200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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