Variant report

Variant rs375154126
Chromosome Location chr21:47498302-47498303
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47485200-47517400 Weak transcription Right Atrium heart
2 chr21:47489400-47511000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr21:47489600-47499200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr21:47489600-47511000 Weak transcription H9 Cell Line embryonic stem cell
5 chr21:47491200-47499000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr21:47492800-47498400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr21:47497600-47504800 Enhancers NHDF-Ad bronchial
8 chr21:47498000-47498400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr21:47498000-47498600 Genic enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr21:47498000-47498600 Enhancers Stomach Smooth Muscle stomach
11 chr21:47498000-47499200 Enhancers Osteobl bone
12 chr21:47498200-47499000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr21:47498200-47499400 Enhancers Adipose Nuclei Adipose
14 chr21:47498200-47499600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
15 chr21:47498200-47500800 Bivalent Enhancer Fetal Muscle Trunk muscle
16 chr21:47498200-47504600 Enhancers Fetal Muscle Leg muscle

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