Variant report

Variant rs371202595
Chromosome Location chr18:44775210-44775211
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:44772800-44775400 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
2 chr18:44774800-44775400 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr18:44774800-44775400 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
4 chr18:44774800-44775400 Enhancers Gastric stomach
5 chr18:44774800-44775600 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
6 chr18:44774800-44775600 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
7 chr18:44774800-44775600 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
8 chr18:44774800-44775600 ZNF genes & repeats Pancreas Pancrea
9 chr18:44775000-44775600 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
10 chr18:44775000-44775800 Bivalent Enhancer H1 Cell Line embryonic stem cell
11 chr18:44775200-44775400 Bivalent Enhancer H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr18:44775200-44775600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin

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