Variant report

Variant rs1360951
Chromosome Location chr10:89892576-89892577
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:89879200-89896600 Weak transcription H9 Cell Line embryonic stem cell
2 chr10:89881200-89903800 Weak transcription Primary B cells from cord blood blood
3 chr10:89891000-89892600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr10:89891000-89892600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr10:89891600-89892600 Active TSS Skeletal Muscle Male skeletal muscle
6 chr10:89891800-89893800 Weak transcription Aorta Aorta
7 chr10:89891800-89894200 Active TSS Skeletal Muscle Female skeletal muscle
8 chr10:89892000-89895000 Weak transcription Adipose Nuclei Adipose
9 chr10:89892200-89895200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr10:89892200-89895400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr10:89892200-89896200 Weak transcription Fetal Thymus thymus
12 chr10:89892200-89896200 Weak transcription Psoas Muscle Psoas
13 chr10:89892400-89892800 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr10:89892400-89896200 Weak transcription Gastric stomach
15 chr10:89892400-89898000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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