Variant report

Variant rs11013478
Chromosome Location chr10:23721465-23721466
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:23719600-23722200 Enhancers Stomach Mucosa stomach
2 chr10:23720200-23723800 Enhancers Primary monocytes fromperipheralblood blood
3 chr10:23720600-23721800 Enhancers NHEK skin
4 chr10:23720800-23722000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr10:23720800-23722000 Enhancers Rectal Mucosa Donor 31 rectum
6 chr10:23721000-23721800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr10:23721000-23721800 Enhancers HMEC breast
8 chr10:23721000-23722000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr10:23721000-23722000 Enhancers Primary neutrophils fromperipheralblood blood
10 chr10:23721000-23722000 Enhancers Rectal Mucosa Donor 29 rectum
11 chr10:23721400-23721600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
12 chr10:23721400-23721800 Active TSS Primary B cells from cord blood blood
13 chr10:23721400-23721800 Flanking Active TSS Hela-S3 cervix
14 chr10:23721400-23722000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr10:23721400-23727400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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