The 2.0 version of rSNPBase

Variant report

Variant esv1178703
Chromosome Location chr9:13486486-13486488
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:13476200-13487200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:13477800-13491800 Weak transcription Right Ventricle heart
3 chr9:13481000-13490000 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr9:13481000-13491800 Weak transcription Pancreas Pancrea
5 chr9:13483000-13487800 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr9:13484600-13491400 Weak transcription Aorta Aorta
7 chr9:13484600-13491800 Weak transcription Left Ventricle heart
8 chr9:13484600-13493600 Weak transcription Right Atrium heart
9 chr9:13485200-13492000 Weak transcription Fetal Muscle Leg muscle
10 chr9:13485600-13489000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr9:13485600-13490600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr9:13485800-13487000 Weak transcription Colon Smooth Muscle Colon
13 chr9:13485800-13487400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr9:13485800-13488000 Weak transcription Fetal Heart heart
15 chr9:13486200-13487200 Weak transcription HMEC breast
16 chr9:13486200-13490200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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Last update: Aug 31, 2015