Variant report

Variant rs2039188
Chromosome Location chr9:16752822-16752823
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:16745400-16758000 Weak transcription Ovary ovary
2 chr9:16745400-16774800 Weak transcription Osteobl bone
3 chr9:16745600-16766200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr9:16749600-16755000 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr9:16750000-16755200 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr9:16750000-16756000 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr9:16750000-16756600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr9:16750600-16755200 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr9:16752200-16753000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr9:16752200-16753000 Enhancers Muscle Satellite Cultured Cells --
11 chr9:16752200-16753000 Enhancers Fetal Lung lung
12 chr9:16752200-16753200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr9:16752400-16754200 Enhancers Colon Smooth Muscle Colon
14 chr9:16752600-16754000 Enhancers NHDF-Ad bronchial
15 chr9:16752800-16754000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr9:16752800-16754400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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