Variant report

Variant rs57455400
Chromosome Location chr10:50569937-50569938
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:50567200-50571600 Enhancers Primary monocytes fromperipheralblood blood
2 chr10:50567600-50572000 Enhancers Pancreas Pancrea
3 chr10:50567800-50570200 Enhancers Right Ventricle heart
4 chr10:50568000-50570600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr10:50568800-50573400 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr10:50569000-50570200 Weak transcription HepG2 liver
7 chr10:50569000-50571000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr10:50569200-50570000 Enhancers Fetal Muscle Trunk muscle
9 chr10:50569400-50570000 Enhancers NHEK skin
10 chr10:50569400-50570600 Bivalent Enhancer Fetal Muscle Leg muscle
11 chr10:50569400-50575600 Weak transcription Right Atrium heart
12 chr10:50569600-50570400 Weak transcription Left Ventricle heart
13 chr10:50569600-50571600 Enhancers Monocytes-CD14+_RO01746 blood
14 chr10:50569600-50575800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr10:50569600-50577200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr10:50569800-50570000 Enhancers Lung lung
17 chr10:50569800-50572000 Enhancers Primary Natural Killer cells fromperipheralblood blood
18 chr10:50569800-50572200 Enhancers GM12878-XiMat blood

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