Variant report

Variant rs577312525
Chromosome Location chr13:53774649-53774650
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:53773400-53775400 Weak transcription Brain Anterior Caudate brain
2 chr13:53773800-53774800 Bivalent Enhancer Fetal Brain Female brain
3 chr13:53774000-53774800 Bivalent Enhancer Brain Germinal Matrix brain
4 chr13:53774200-53776200 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr13:53774200-53776200 ZNF genes & repeats Spleen Spleen
6 chr13:53774200-53776600 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
7 chr13:53774400-53775200 Transcr. at gene 5' and 3' iPS DF 19.11 Cell Line embryonic stem cell
8 chr13:53774400-53776600 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
9 chr13:53774400-53776600 Enhancers Pancreas Pancrea
10 chr13:53774600-53774800 Bivalent Enhancer H1 Cell Line embryonic stem cell
11 chr13:53774600-53774800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
12 chr13:53774600-53775200 Flanking Bivalent TSS/Enh ES-UCSF4 Cell Line embryonic stem cell
13 chr13:53774600-53775400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr13:53774600-53776000 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
15 chr13:53774600-53776000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell

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