Variant report

Variant rs73033786
Chromosome Location chr2:180299692-180299693
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180293800-180307800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr2:180294200-180306600 Weak transcription Liver Liver
3 chr2:180294200-180307400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr2:180294600-180305600 Weak transcription H1 Cell Line embryonic stem cell
5 chr2:180299000-180300000 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr2:180299200-180300200 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr2:180299200-180300400 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr2:180299400-180299800 Enhancers H9 Cell Line embryonic stem cell
9 chr2:180299400-180300400 Enhancers HUES48 Cell Line embryonic stem cell
10 chr2:180299400-180300400 Enhancers HUES6 Cell Line embryonic stem cell
11 chr2:180299400-180300400 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr2:180299600-180299800 Flanking Active TSS NHDF-Ad bronchial
13 chr2:180299600-180300000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr2:180299600-180300200 Enhancers HUES64 Cell Line embryonic stem cell

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