Variant report

Variant rs6824528
Chromosome Location chr4:22366066-22366067
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:22329000-22389400 Weak transcription Pancreas Pancrea
2 chr4:22336600-22385400 Weak transcription Fetal Intestine Large intestine
3 chr4:22354000-22378200 Weak transcription Aorta Aorta
4 chr4:22362400-22366400 Weak transcription Ovary ovary
5 chr4:22364000-22366200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr4:22364000-22366400 Enhancers Muscle Satellite Cultured Cells --
7 chr4:22364400-22366600 Enhancers Osteobl bone
8 chr4:22364800-22366400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr4:22365000-22366400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr4:22365600-22386800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr4:22365800-22384600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr4:22366000-22371400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
13 chr4:22366000-22385000 Weak transcription NHEK skin

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