Variant report

Variant rs9579515
Chromosome Location chr13:30590288-30590289
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:30581000-30592000 Weak transcription HUES6 Cell Line embryonic stem cell
2 chr13:30587200-30593400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr13:30588800-30594200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr13:30589400-30590400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr13:30589400-30590600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr13:30589800-30590400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr13:30589800-30592000 Weak transcription H1 Cell Line embryonic stem cell
8 chr13:30589800-30592000 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr13:30589800-30593600 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr13:30589800-30593800 Weak transcription H9 Cell Line embryonic stem cell
11 chr13:30589800-30594200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
12 chr13:30590000-30592000 Weak transcription Placenta Amnion Placenta Amnion
13 chr13:30590200-30590400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr13:30590200-30590600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
15 chr13:30590200-30591000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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