Variant report

Variant rs2151660
Chromosome Location chr9:13489422-13489423
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr9:13484600-13491400 Weak transcription Aorta Aorta
5 chr9:13484600-13491800 Weak transcription Left Ventricle heart
6 chr9:13484600-13493600 Weak transcription Right Atrium heart
7 chr9:13485200-13492000 Weak transcription Fetal Muscle Leg muscle
8 chr9:13485600-13490600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr9:13486200-13490200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr9:13487200-13490000 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr9:13487600-13489800 Weak transcription iPS-15b Cell Line embryonic stem cell
12 chr9:13488200-13490000 Weak transcription H9 Cell Line embryonic stem cell
13 chr9:13488200-13490200 Weak transcription ES-WA7 Cell Line embryonic stem cell
14 chr9:13488200-13495000 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr9:13488800-13491000 Weak transcription HMEC breast
16 chr9:13488800-13491400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
17 chr9:13489000-13491800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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