Variant report

Variant rs9588032
Chromosome Location chr13:110570720-110570721
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:110566200-110572000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr13:110566800-110590400 Weak transcription Aorta Aorta
3 chr13:110569000-110571200 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr13:110569400-110570800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr13:110569400-110573400 Enhancers HSMM muscle
6 chr13:110569600-110572400 Enhancers HSMMtube muscle
7 chr13:110569600-110573000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr13:110569800-110570800 Weak transcription Adipose Nuclei Adipose
9 chr13:110569800-110570800 Weak transcription Skeletal Muscle Male skeletal muscle
10 chr13:110570400-110571200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr13:110570400-110571200 Enhancers Colon Smooth Muscle Colon
12 chr13:110570400-110571400 Flanking Active TSS Muscle Satellite Cultured Cells --
13 chr13:110570400-110571400 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr13:110570600-110570800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr13:110570600-110570800 Enhancers NHDF-Ad bronchial
16 chr13:110570600-110571200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr13:110570600-110571400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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