Variant report

Variant rs2844658
Chromosome Location chr6:30825812-30825813
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:30823200-30826400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
2 chr6:30823600-30826400 Enhancers Fetal Thymus thymus
3 chr6:30823600-30835400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr6:30824400-30826000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr6:30824400-30826200 Enhancers Fetal Lung lung
6 chr6:30824600-30826000 Enhancers Fetal Stomach stomach
7 chr6:30825000-30826200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr6:30825000-30826200 Bivalent Enhancer Placenta Placenta
9 chr6:30825200-30826000 Flanking Active TSS GM12878-XiMat blood
10 chr6:30825600-30826000 Enhancers HepG2 liver
11 chr6:30825600-30826400 Enhancers Fetal Kidney kidney

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