Variant report

Variant rs2810474
Chromosome Location chr9:136862150-136862151
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:136859600-136864800 Weak transcription Fetal Lung lung
2 chr9:136859600-136875400 Weak transcription Spleen Spleen
3 chr9:136860000-136864000 Weak transcription Brain Germinal Matrix brain
4 chr9:136860200-136864200 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr9:136860200-136865200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr9:136860400-136862800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr9:136860400-136862800 Weak transcription Fetal Brain Male brain
8 chr9:136860400-136864000 Weak transcription Fetal Brain Female brain
9 chr9:136860600-136863400 Weak transcription HSMM muscle
10 chr9:136861000-136864800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr9:136861200-136862400 Enhancers HSMMtube muscle
12 chr9:136861200-136862800 Enhancers Fetal Muscle Leg muscle
13 chr9:136861600-136862200 Bivalent Enhancer Fetal Muscle Trunk muscle
14 chr9:136861800-136862200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
15 chr9:136862000-136862200 Active TSS H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr9:136862000-136862200 Enhancers Breast Myoepithelial Primary Cells Breast
17 chr9:136862000-136862200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
18 chr9:136862000-136862200 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
19 chr9:136862000-136862600 Enhancers Pancreas Pancrea

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