Variant report

Variant rs12069743
Chromosome Location chr1:180206635-180206636
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180204600-180209200 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr1:180204800-180209000 Flanking Bivalent TSS/Enh iPS-18 Cell Line embryonic stem cell
3 chr1:180205000-180206800 Flanking Bivalent TSS/Enh HUES64 Cell Line embryonic stem cell
4 chr1:180205000-180208000 Flanking Bivalent TSS/Enh HUES48 Cell Line embryonic stem cell
5 chr1:180205000-180208800 Flanking Bivalent TSS/Enh iPS-20b Cell Line embryonic stem cell
6 chr1:180205400-180206800 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
7 chr1:180205400-180206800 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
8 chr1:180206000-180207000 Flanking Bivalent TSS/Enh H1 Cell Line embryonic stem cell
9 chr1:180206200-180207000 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
10 chr1:180206200-180207000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr1:180206400-180207000 Bivalent Enhancer H9 Cell Line embryonic stem cell
12 chr1:180206600-180208200 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
13 chr1:180206600-180209200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell

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