Variant report

Variant rs374785198
Chromosome Location chr1:161409038-161409039
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:161408800-161409200 Enhancers K562 blood
2 chr1:161409000-161409200 Flanking Bivalent TSS/Enh H9 Cell Line embryonic stem cell
3 chr1:161409000-161409200 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
4 chr1:161409000-161409200 Bivalent/Poised TSS Primary hematopoietic stem cells blood
5 chr1:161409000-161409200 Enhancers Hela-S3 cervix
6 chr1:161409000-161409600 Bivalent/Poised TSS H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr1:161409000-161409600 Bivalent Enhancer HepG2 liver
8 chr1:161409000-161409800 Enhancers Pancreas Pancrea
9 chr1:161409000-161410000 Bivalent/Poised TSS ES-WA7 Cell Line embryonic stem cell
10 chr1:161409000-161410600 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell

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