Variant report

Variant rs35883476
Chromosome Location chr6:28368508-28368509
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:28366800-28368600 Active TSS Aorta Aorta
2 chr6:28368000-28370800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr6:28368200-28368600 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
4 chr6:28368200-28368600 Flanking Active TSS GM12878-XiMat blood
5 chr6:28368200-28368600 Flanking Active TSS K562 blood
6 chr6:28368200-28369000 Enhancers Muscle Satellite Cultured Cells --
7 chr6:28368200-28369000 Enhancers NHEK skin
8 chr6:28368200-28369400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr6:28368400-28368600 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
10 chr6:28368400-28368600 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
11 chr6:28368400-28368600 Bivalent Enhancer Primary B cells from cord blood blood
12 chr6:28368400-28368600 Enhancers Dnd41 blood
13 chr6:28368400-28368600 Enhancers HepG2 liver
14 chr6:28368400-28368800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr6:28368400-28369600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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