Variant report

Variant rs142292768
Chromosome Location chr9:2965382-2965383
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:2961600-2969000 Enhancers NHDF-Ad bronchial
2 chr9:2962800-2966600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr9:2963200-2968000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr9:2963600-2966400 Weak transcription Fetal Brain Female brain
5 chr9:2964000-2965800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr9:2964000-2967400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr9:2964400-2965800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr9:2964400-2966600 Weak transcription Fetal Stomach stomach
9 chr9:2964400-2966800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr9:2965000-2965600 Enhancers Fetal Brain Male brain
11 chr9:2965200-2966400 Weak transcription Adipose Nuclei Adipose

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