Variant report

Variant rs73978911
Chromosome Location chr2:190957642-190957643
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:190939600-190960200 Weak transcription Aorta Aorta
2 chr2:190950800-190958400 Weak transcription Fetal Intestine Large intestine
3 chr2:190954400-190958400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr2:190954800-190970400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr2:190955000-190958400 Weak transcription Brain Hippocampus Middle brain
6 chr2:190955200-190958400 Weak transcription Brain Substantia Nigra brain
7 chr2:190955800-190958800 Weak transcription Fetal Intestine Small intestine
8 chr2:190957200-190958400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
9 chr2:190957200-190958600 Weak transcription Fetal Lung lung
10 chr2:190957400-190958400 Weak transcription Stomach Mucosa stomach
11 chr2:190957400-190958600 Weak transcription Duodenum Mucosa Duodenum

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