Variant report

Variant rs9550556
Chromosome Location chr13:30903964-30903965
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:30882200-30910800 Weak transcription Primary T regulatory cells fromperipheralblood blood
2 chr13:30882400-30905400 Weak transcription Right Ventricle heart
3 chr13:30882400-30905400 Weak transcription Stomach Smooth Muscle stomach
4 chr13:30888000-30909600 Weak transcription Thymus Thymus
5 chr13:30889400-30906400 Weak transcription Primary B cells from cord blood blood
6 chr13:30892800-30913400 Weak transcription Psoas Muscle Psoas
7 chr13:30894800-30905400 Weak transcription Brain Anterior Caudate brain
8 chr13:30897200-30905600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr13:30901800-30905400 Weak transcription Fetal Muscle Leg muscle
10 chr13:30902400-30904800 Enhancers Dnd41 blood
11 chr13:30903400-30904400 Enhancers Fetal Thymus thymus
12 chr13:30903600-30904600 Enhancers Fetal Intestine Small intestine
13 chr13:30903600-30914000 Weak transcription Aorta Aorta
14 chr13:30903800-30904000 Enhancers Colon Smooth Muscle Colon
15 chr13:30903800-30905000 Weak transcription Fetal Stomach stomach
16 chr13:30903800-30905200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr13:30903800-30905400 Weak transcription Fetal Heart heart
18 chr13:30903800-30905600 Weak transcription Primary B cells from peripheral blood blood
19 chr13:30903800-30906600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
20 chr13:30903800-30912000 Weak transcription NHDF-Ad bronchial

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