Variant report

Variant rs73403938
Chromosome Location chr11:10369800-10369801
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:10348200-10370200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr11:10367400-10372000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr11:10368200-10370200 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr11:10368400-10369800 Weak transcription HSMM muscle
5 chr11:10368800-10373000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr11:10369600-10374200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr11:10369800-10371400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr11:10369800-10373000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr11:10369800-10373000 Enhancers Adipose Nuclei Adipose
10 chr11:10369800-10374000 Enhancers HSMM muscle
11 chr11:10369800-10374000 Enhancers NHDF-Ad bronchial
12 chr11:10369800-10374200 Enhancers NHLF lung
13 chr11:10369800-10378000 Enhancers Placenta Placenta

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