Variant report

Variant rs12248638
Chromosome Location chr10:3955976-3955977
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:3928200-3981400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:3950000-3957000 Weak transcription Lung lung
3 chr10:3950200-3957000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr10:3954400-3957000 Weak transcription Skeletal Muscle Female skeletal muscle
5 chr10:3954400-3961400 Weak transcription Aorta Aorta
6 chr10:3954400-3963800 Weak transcription Esophagus oesophagus
7 chr10:3954600-3956400 Weak transcription Rectal Smooth Muscle rectum
8 chr10:3954600-3957200 Flanking Active TSS Fetal Heart heart
9 chr10:3954600-3966000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr10:3955000-3956000 Flanking Active TSS NHEK skin
11 chr10:3955200-3956200 Enhancers Fetal Muscle Leg muscle
12 chr10:3955200-3961000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr10:3955400-3956000 Flanking Active TSS Left Ventricle heart
14 chr10:3955400-3957400 Enhancers Colon Smooth Muscle Colon
15 chr10:3955400-3958400 Weak transcription Right Atrium heart
16 chr10:3955600-3956000 Active TSS Right Ventricle heart
17 chr10:3955600-3956000 Bivalent Enhancer HepG2 liver
18 chr10:3955600-3956600 Weak transcription Stomach Smooth Muscle stomach
19 chr10:3955600-3957000 Weak transcription Fetal Muscle Trunk muscle
20 chr10:3955600-3966000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
21 chr10:3955800-3957400 Enhancers Breast Myoepithelial Primary Cells Breast

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