Variant report

Variant rs375911037
Chromosome Location chr12:9504449-9504450
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:9498600-9505000 Strong transcription Fetal Lung lung
2 chr12:9499000-9506000 Weak transcription Primary T helper naive cells from peripheral blood blood
3 chr12:9501800-9504600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr12:9502800-9507200 Weak transcription Fetal Heart heart
5 chr12:9503200-9506000 Weak transcription Stomach Smooth Muscle stomach
6 chr12:9503400-9506000 Enhancers HepG2 liver
7 chr12:9503800-9504800 Weak transcription Fetal Thymus thymus
8 chr12:9503800-9505800 Weak transcription Thymus Thymus
9 chr12:9504000-9504600 Weak transcription HMEC breast
10 chr12:9504000-9505200 Strong transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr12:9504200-9505000 Weak transcription Primary hematopoietic stem cells blood
12 chr12:9504400-9506800 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin03 Skin

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