Variant report

Variant rs117428165
Chromosome Location chr9:117086549-117086550
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117051200-117097200 Weak transcription Placenta Amnion Placenta Amnion
2 chr9:117051400-117086800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr9:117059000-117089800 Weak transcription H1 Cell Line embryonic stem cell
4 chr9:117061000-117110000 Weak transcription A549 lung
5 chr9:117073400-117086800 Weak transcription Spleen Spleen
6 chr9:117079400-117090200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr9:117082200-117098600 Weak transcription Brain Germinal Matrix brain
8 chr9:117084800-117092800 Weak transcription Ovary ovary
9 chr9:117085000-117088200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr9:117085000-117097600 Weak transcription Fetal Lung lung
11 chr9:117085400-117086800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
12 chr9:117085800-117086600 Active TSS Primary B cells from cord blood blood
13 chr9:117086000-117087600 Transcr. at gene 5' and 3' Liver Liver
14 chr9:117086200-117087200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
15 chr9:117086200-117090000 Weak transcription Monocytes-CD14+_RO01746 blood
16 chr9:117086400-117087600 Transcr. at gene 5' and 3' HepG2 liver

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