Variant report

Variant rs12124515
Chromosome Location chr1:170452501-170452502
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:170450600-170455600 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr1:170451200-170456600 Weak transcription Dnd41 blood
3 chr1:170451200-170457200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr1:170452000-170452800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr1:170452000-170453200 Enhancers NHDF-Ad bronchial
6 chr1:170452400-170452600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr1:170452400-170452600 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
8 chr1:170452400-170453000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr1:170452400-170453000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr1:170452400-170453000 Enhancers Fetal Stomach stomach

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