Variant report

Variant rs13392521
Chromosome Location chr2:37407303-37407304
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:37406200-37407800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr2:37406600-37408000 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr2:37406800-37407800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:37406800-37407800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr2:37407000-37407400 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
6 chr2:37407000-37407400 Bivalent Enhancer HepG2 liver
7 chr2:37407000-37407600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr2:37407000-37407600 Enhancers HMEC breast
9 chr2:37407000-37407600 Enhancers NHEK skin
10 chr2:37407000-37407800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr2:37407000-37408000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr2:37407000-37408000 Enhancers Adipose Nuclei Adipose
13 chr2:37407200-37407400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr2:37407200-37407400 Enhancers iPS-20b Cell Line embryonic stem cell
15 chr2:37407200-37407600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr2:37407200-37408000 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
17 chr2:37407200-37409600 Enhancers HUES48 Cell Line embryonic stem cell

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