Variant report

Variant rs6475581
Chromosome Location chr9:21788877-21788878
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21786800-21789200 Weak transcription Primary neutrophils fromperipheralblood blood
2 chr9:21787600-21789200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr9:21787800-21789000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr9:21787800-21789800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr9:21788200-21789800 Enhancers HMEC breast
6 chr9:21788200-21790200 Enhancers Hela-S3 cervix
7 chr9:21788200-21790200 Enhancers NHEK skin
8 chr9:21788600-21789000 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr9:21788600-21789000 Active TSS Stomach Mucosa stomach
10 chr9:21788600-21789400 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr9:21788600-21789400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr9:21788600-21789600 Flanking Active TSS A549 lung
13 chr9:21788600-21789800 Enhancers NH-A brain
14 chr9:21788800-21789000 Enhancers Duodenum Smooth Muscle Duodenum
15 chr9:21788800-21789000 Active TSS Fetal Intestine Small intestine
16 chr9:21788800-21789000 Enhancers NHLF lung
17 chr9:21788800-21789000 Flanking Active TSS Osteobl bone
18 chr9:21788800-21789600 Enhancers NHDF-Ad bronchial

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