Variant report

Variant rs529662906
Chromosome Location chr17:37765269-37765270
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:37763600-37773600 Weak transcription Gastric stomach
2 chr17:37764000-37765400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
3 chr17:37764000-37765400 Bivalent Enhancer A549 lung
4 chr17:37764400-37765600 Bivalent Enhancer Fetal Brain Male brain
5 chr17:37764800-37765400 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
6 chr17:37764800-37765400 Enhancers K562 blood
7 chr17:37765000-37765400 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr17:37765000-37765400 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
9 chr17:37765000-37765600 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
10 chr17:37765200-37765400 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
11 chr17:37765200-37765400 Flanking Active TSS Fetal Brain Female brain

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