Variant report

Variant rs59065063
Chromosome Location chr4:53843982-53843983
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:53786600-53861400 Weak transcription Primary B cells from cord blood blood
2 chr4:53818200-53849800 Weak transcription Primary T cells from cord blood blood
3 chr4:53838800-53850200 Weak transcription Aorta Aorta
4 chr4:53842800-53848400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr4:53843000-53844400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr4:53843000-53844600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr4:53843200-53847800 Weak transcription Fetal Heart heart
8 chr4:53843400-53844000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr4:53843600-53844400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr4:53843600-53844400 Enhancers Fetal Kidney kidney
11 chr4:53843600-53844400 Enhancers Fetal Stomach stomach
12 chr4:53843600-53845200 Enhancers Placenta Placenta
13 chr4:53843800-53844200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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