Variant report

Variant rs7908831
Chromosome Location chr10:93331127-93331128
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:93315200-93335600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr10:93323200-93338000 Weak transcription HSMMtube muscle
3 chr10:93323400-93334600 Weak transcription Pancreas Pancrea
4 chr10:93324400-93341800 Weak transcription Aorta Aorta
5 chr10:93325800-93334800 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr10:93326200-93334200 Weak transcription Left Ventricle heart
7 chr10:93327800-93335600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr10:93327800-93347400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr10:93328400-93335400 Weak transcription HMEC breast
10 chr10:93328600-93332200 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr10:93328600-93332600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr10:93329600-93331400 Weak transcription HSMM muscle
13 chr10:93330400-93335000 Weak transcription K562 blood
14 chr10:93330600-93333400 Weak transcription Fetal Heart heart
15 chr10:93331000-93331800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr10:93331000-93331800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
17 chr10:93331000-93332000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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