Variant report

Variant rs190043710
Chromosome Location chr9:95439581-95439582
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:95433400-95442800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr9:95433800-95441800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr9:95433800-95444000 Weak transcription Fetal Brain Female brain
4 chr9:95434000-95439800 Weak transcription Brain Germinal Matrix brain
5 chr9:95434000-95441800 Weak transcription H9 Cell Line embryonic stem cell
6 chr9:95434000-95441800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr9:95434000-95442400 Weak transcription NHDF-Ad bronchial
8 chr9:95434200-95441800 Weak transcription Esophagus oesophagus
9 chr9:95434200-95441800 Weak transcription NHEK skin
10 chr9:95434200-95442800 Weak transcription Placenta Placenta
11 chr9:95436800-95439600 Weak transcription ES-I3 Cell Line embryonic stem cell
12 chr9:95438600-95439600 Enhancers K562 blood
13 chr9:95439000-95440800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
14 chr9:95439200-95439600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr9:95439200-95439600 Enhancers Primary T cells from cord blood blood
16 chr9:95439200-95439600 Enhancers Primary hematopoietic stem cells short term culture blood
17 chr9:95439200-95439800 Enhancers Fetal Thymus thymus
18 chr9:95439400-95439600 Enhancers HepG2 liver

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