Variant report

Variant rs10877779
Chromosome Location chr12:40309397-40309398
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:40298400-40314200 Weak transcription Fetal Kidney kidney
2 chr12:40298800-40311200 Weak transcription Pancreas Pancrea
3 chr12:40303200-40312200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr12:40307800-40309800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr12:40309200-40309400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr12:40309200-40309800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr12:40309200-40310000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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