Variant report

Variant rs567393347
Chromosome Location chr21:47053053-47053054
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr21:47051200-47053200 Enhancers Primary B cells from peripheral blood blood
3 chr21:47051600-47053200 Flanking Active TSS Thymus Thymus
4 chr21:47052600-47053200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr21:47052600-47053200 Enhancers Spleen Spleen
6 chr21:47052600-47059000 Weak transcription Primary T helper cells fromperipheralblood blood
7 chr21:47052800-47053200 Enhancers Esophagus oesophagus
8 chr21:47052800-47053200 Enhancers GM12878-XiMat blood
9 chr21:47052800-47053200 Enhancers HMEC breast
10 chr21:47052800-47058000 Weak transcription Primary T helper naive cells fromperipheralblood blood
11 chr21:47052800-47058400 Weak transcription Primary T cells from cord blood blood
12 chr21:47053000-47054200 Enhancers Fetal Thymus thymus
13 chr21:47053000-47058000 Weak transcription Dnd41 blood

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