Variant report

Variant rs573541735
Chromosome Location chr1:184987179-184987180
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:184984000-184987600 Enhancers Fetal Intestine Large intestine
2 chr1:184984600-184987400 Enhancers K562 blood
3 chr1:184985000-184987200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr1:184985600-184987400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:184985800-184987400 Enhancers HMEC breast
6 chr1:184985800-184987400 Enhancers NHDF-Ad bronchial
7 chr1:184985800-184987600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr1:184986000-184987200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr1:184986000-184987200 Enhancers Monocytes-CD14+_RO01746 blood
10 chr1:184986200-184987400 Enhancers HSMM muscle
11 chr1:184986600-184987200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr1:184986600-184987200 Enhancers A549 lung
13 chr1:184987000-184987600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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