Variant report

Variant rs7857231
Chromosome Location chr9:118617719-118617720
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:118613600-118617800 Weak transcription HSMM muscle
2 chr9:118613800-118618000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr9:118613800-118618000 Weak transcription NHDF-Ad bronchial
4 chr9:118613800-118618000 Weak transcription NHLF lung
5 chr9:118613800-118618200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr9:118616800-118617800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr9:118617600-118618000 Enhancers A549 lung
8 chr9:118617600-118618600 Enhancers HUES6 Cell Line embryonic stem cell
9 chr9:118617600-118618600 Enhancers HUES64 Cell Line embryonic stem cell
10 chr9:118617600-118618600 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr9:118617600-118618600 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr9:118617600-118619000 Enhancers iPS-15b Cell Line embryonic stem cell
13 chr9:118617600-118619200 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr9:118617600-118619200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr9:118617600-118619200 Enhancers HUES48 Cell Line embryonic stem cell

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