Variant report

Variant rs556689727
Chromosome Location chr21:47054717-47054718
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47050400-47055800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr21:47052600-47059000 Weak transcription Primary T helper cells fromperipheralblood blood
3 chr21:47052800-47058000 Weak transcription Primary T helper naive cells fromperipheralblood blood
4 chr21:47052800-47058400 Weak transcription Primary T cells from cord blood blood
5 chr21:47053000-47058000 Weak transcription Dnd41 blood
6 chr21:47053200-47055400 Weak transcription Esophagus oesophagus
7 chr21:47053200-47055800 Weak transcription Spleen Spleen
8 chr21:47054200-47055000 Flanking Active TSS Fetal Thymus thymus
9 chr21:47054400-47054800 Active TSS NHDF-Ad bronchial
10 chr21:47054400-47055000 Active TSS HSMMtube muscle
11 chr21:47054400-47055200 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
12 chr21:47054400-47055200 Enhancers HSMM muscle
13 chr21:47054400-47055200 Enhancers Osteobl bone
14 chr21:47054400-47055400 Enhancers Primary B cells from peripheral blood blood
15 chr21:47054400-47056200 Enhancers Gastric stomach
16 chr21:47054600-47054800 Bivalent/Poised TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr21:47054600-47054800 Bivalent/Poised TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
18 chr21:47054600-47054800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
19 chr21:47054600-47054800 Flanking Active TSS Thymus Thymus
20 chr21:47054600-47054800 Active TSS GM12878-XiMat blood
21 chr21:47054600-47055000 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin01 Skin

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