Variant report

Variant rs572269491
Chromosome Location chr20:14677997-14677998
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14668400-14680800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr20:14668800-14678000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr20:14674800-14681400 Weak transcription Pancreas Pancrea
4 chr20:14676400-14681200 Weak transcription GM12878-XiMat blood
5 chr20:14677000-14678000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr20:14677200-14678600 Enhancers Adipose Nuclei Adipose
7 chr20:14677200-14678800 Enhancers Colon Smooth Muscle Colon
8 chr20:14677600-14678000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr20:14677600-14678200 Enhancers Rectal Smooth Muscle rectum
10 chr20:14677600-14678800 Enhancers Liver Liver
11 chr20:14677800-14678000 Enhancers Fetal Lung lung
12 chr20:14677800-14678000 Enhancers NHEK skin
13 chr20:14677800-14678200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr20:14677800-14679600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr20:14677800-14681000 Weak transcription Fetal Kidney kidney
16 chr20:14677800-14681200 Weak transcription Fetal Heart heart
17 chr20:14677800-14681600 Weak transcription Rectal Mucosa Donor 31 rectum

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