Variant report

Variant rs558870548
Chromosome Location chr1:228657940-228657941
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:228653800-228660600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:228656800-228659800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
3 chr1:228657200-228658000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
4 chr1:228657200-228658400 Enhancers HUES48 Cell Line embryonic stem cell
5 chr1:228657400-228658000 Flanking Bivalent TSS/Enh H1 Cell Line embryonic stem cell
6 chr1:228657600-228658000 Enhancers HUES64 Cell Line embryonic stem cell
7 chr1:228657800-228658000 Bivalent/Poised TSS Fetal Brain Female brain
8 chr1:228657800-228659800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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