Variant report

Variant rs10768001
Chromosome Location chr11:33233486-33233487
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:33229600-33235200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
2 chr11:33232600-33233800 Enhancers HepG2 liver
3 chr11:33233000-33233600 Flanking Active TSS Primary monocytes fromperipheralblood blood
4 chr11:33233000-33233600 Enhancers Brain Substantia Nigra brain
5 chr11:33233000-33233800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr11:33233200-33233600 Flanking Active TSS Primary neutrophils fromperipheralblood blood
7 chr11:33233200-33233600 Flanking Active TSS Adipose Nuclei Adipose
8 chr11:33233200-33233800 Enhancers Primary B cells from cord blood blood
9 chr11:33233200-33233800 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr11:33233200-33233800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
11 chr11:33233400-33233600 Enhancers Brain Cingulate Gyrus brain
12 chr11:33233400-33233600 Enhancers Spleen Spleen
13 chr11:33233400-33233800 Enhancers Placenta Placenta
14 chr11:33233400-33234400 Enhancers Pancreas Pancrea

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