Variant report

Variant rs184169486
Chromosome Location chr1:46951824-46951825
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:46933200-46955000 Weak transcription Right Atrium heart
2 chr1:46951000-46952000 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
3 chr1:46951000-46952000 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
4 chr1:46951200-46952000 Bivalent/Poised TSS iPS-18 Cell Line embryonic stem cell
5 chr1:46951200-46952800 Weak transcription K562 blood
6 chr1:46951200-46957200 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
7 chr1:46951600-46952000 Flanking Bivalent TSS/Enh H1 Cell Line embryonic stem cell
8 chr1:46951800-46952000 Flanking Bivalent TSS/Enh H9 Cell Line embryonic stem cell
9 chr1:46951800-46952000 Flanking Bivalent TSS/Enh HUES48 Cell Line embryonic stem cell
10 chr1:46951800-46952000 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
11 chr1:46951800-46952000 Flanking Bivalent TSS/Enh HUES64 Cell Line embryonic stem cell
12 chr1:46951800-46952000 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
13 chr1:46951800-46952200 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
14 chr1:46951800-46953800 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
15 chr1:46951800-46954200 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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