Variant report

Variant rs182076771
Chromosome Location chr10:90017029-90017030
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:90005800-90017200 Weak transcription Rectal Mucosa Donor 31 rectum
2 chr10:90014200-90018400 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr10:90014200-90028400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr10:90014400-90017400 Weak transcription HUVEC blood vessel
5 chr10:90014400-90019800 Weak transcription GM12878-XiMat blood
6 chr10:90014600-90019800 Weak transcription Dnd41 blood
7 chr10:90014600-90025600 Weak transcription Osteobl bone
8 chr10:90015000-90020200 Weak transcription HMEC breast
9 chr10:90015200-90020200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr10:90015600-90017200 Weak transcription Fetal Intestine Large intestine
11 chr10:90015800-90018600 Weak transcription Pancreas Pancrea
12 chr10:90016600-90017200 Enhancers Muscle Satellite Cultured Cells --
13 chr10:90016600-90017200 Enhancers Skeletal Muscle Male skeletal muscle
14 chr10:90016600-90017600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr10:90016600-90017600 Enhancers Skeletal Muscle Female skeletal muscle
16 chr10:90016600-90017600 Enhancers NHDF-Ad bronchial
17 chr10:90016600-90017600 Enhancers NHLF lung
18 chr10:90016800-90017200 Weak transcription Adipose Nuclei Adipose
19 chr10:90017000-90017200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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