Variant report

Variant rs28947196
Chromosome Location chr2:113674255-113674256
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113664800-113678000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr2:113671600-113674400 Enhancers Primary Natural Killer cells fromperipheralblood blood
3 chr2:113671600-113674800 Enhancers Primary T cells fromperipheralblood blood
4 chr2:113671600-113683000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr2:113671800-113674600 Enhancers Fetal Thymus thymus
6 chr2:113671800-113675000 Enhancers Thymus Thymus
7 chr2:113672000-113674600 Enhancers Primary T helper naive cells from peripheral blood blood
8 chr2:113672600-113677800 Enhancers Fetal Intestine Small intestine
9 chr2:113672800-113677600 Enhancers Fetal Intestine Large intestine
10 chr2:113674000-113674400 Flanking Active TSS GM12878-XiMat blood
11 chr2:113674200-113679400 Weak transcription Primary T killer memory cells from peripheral blood blood

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