Variant report

Variant rs4838988
Chromosome Location chr1:114058280-114058281
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:114053800-114062200 Weak transcription Gastric stomach
2 chr1:114054200-114062200 Weak transcription Pancreas Pancrea
3 chr1:114057600-114058600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr1:114057600-114058600 Enhancers Muscle Satellite Cultured Cells --
5 chr1:114057600-114063200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr1:114057800-114058600 Weak transcription Placenta Amnion Placenta Amnion
7 chr1:114057800-114058600 Enhancers NH-A brain
8 chr1:114058000-114058600 Enhancers NHEK skin
9 chr1:114058000-114058600 Enhancers Osteobl bone
10 chr1:114058000-114062600 Enhancers HepG2 liver
11 chr1:114058200-114058400 Enhancers HSMM muscle
12 chr1:114058200-114059000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:114058200-114062000 Weak transcription Stomach Mucosa stomach

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