Variant report

Variant rs13292589
Chromosome Location chr9:103249058-103249059
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:103237000-103251600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr9:103238200-103251600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr9:103238200-103252000 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr9:103238200-103264200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr9:103238200-103274600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr9:103238400-103251400 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr9:103238400-103251400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr9:103238400-103251800 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr9:103238600-103251800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr9:103245200-103251600 Weak transcription Brain Substantia Nigra brain
11 chr9:103245400-103251400 Weak transcription iPS-15b Cell Line embryonic stem cell
12 chr9:103247800-103253800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr9:103248000-103252000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
14 chr9:103248200-103251600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
15 chr9:103249000-103249200 Enhancers H1 Cell Line embryonic stem cell
16 chr9:103249000-103249200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
17 chr9:103249000-103251800 Weak transcription Brain Hippocampus Middle brain

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