Variant report

Variant rs535021672
Chromosome Location chr9:13487657-13487658
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:13477800-13491800 Weak transcription Right Ventricle heart
2 chr9:13481000-13490000 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr9:13481000-13491800 Weak transcription Pancreas Pancrea
4 chr9:13483000-13487800 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr9:13484600-13491400 Weak transcription Aorta Aorta
6 chr9:13484600-13491800 Weak transcription Left Ventricle heart
7 chr9:13484600-13493600 Weak transcription Right Atrium heart
8 chr9:13485200-13492000 Weak transcription Fetal Muscle Leg muscle
9 chr9:13485600-13489000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr9:13485600-13490600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr9:13485800-13488000 Weak transcription Fetal Heart heart
12 chr9:13486200-13490200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr9:13487200-13488800 Enhancers HMEC breast
14 chr9:13487200-13489000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr9:13487200-13490000 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr9:13487400-13487800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr9:13487600-13488000 Weak transcription H9 Cell Line embryonic stem cell
18 chr9:13487600-13489800 Weak transcription iPS-15b Cell Line embryonic stem cell

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