Variant report

Variant rs12733479
Chromosome Location chr1:46951059-46951060
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:46933200-46955000 Weak transcription Right Atrium heart
2 chr1:46946000-46951200 Enhancers K562 blood
3 chr1:46950600-46951200 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
4 chr1:46950600-46951400 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr1:46950600-46951400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
6 chr1:46951000-46951200 Flanking Bivalent TSS/Enh H1 Cell Line embryonic stem cell
7 chr1:46951000-46951200 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr1:46951000-46951200 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
9 chr1:46951000-46951200 Flanking Bivalent TSS/Enh iPS-18 Cell Line embryonic stem cell
10 chr1:46951000-46951600 Bivalent/Poised TSS iPS DF 6.9 Cell Line embryonic stem cell
11 chr1:46951000-46951800 Bivalent/Poised TSS H9 Cell Line embryonic stem cell
12 chr1:46951000-46951800 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
13 chr1:46951000-46951800 Bivalent Enhancer Primary T helper cells PMA-I stimulated --
14 chr1:46951000-46951800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:46951000-46951800 Bivalent Enhancer Fetal Stomach stomach
16 chr1:46951000-46952000 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
17 chr1:46951000-46952000 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell

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