Variant report

Variant rs13377956
Chromosome Location chr12:24891174-24891175
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:24887000-24900400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr12:24889600-24893400 Enhancers Fetal Lung lung
3 chr12:24889800-24895800 Enhancers Dnd41 blood
4 chr12:24890200-24892800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr12:24890400-24893200 Weak transcription Primary B cells from peripheral blood blood
6 chr12:24890600-24891800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr12:24890600-24891800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr12:24890600-24892400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr12:24890800-24891200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr12:24890800-24891800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr12:24890800-24891800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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