Variant report

Variant rs28600353
Chromosome Location chr9:12924253-12924254
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:12917000-12933600 Weak transcription iPS-20b Cell Line embryonic stem cell
2 chr9:12917200-12930000 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr9:12917200-12934000 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr9:12917400-12933600 Weak transcription ES-WA7 Cell Line embryonic stem cell
5 chr9:12922000-12925400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr9:12922200-12924800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr9:12922200-12924800 Enhancers Fetal Heart heart
8 chr9:12922200-12925400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:12922200-12925400 Enhancers NHDF-Ad bronchial
10 chr9:12922800-12931000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr9:12923000-12924800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr9:12923200-12924400 Enhancers NHLF lung
13 chr9:12923200-12924400 Enhancers Osteobl bone
14 chr9:12923200-12925400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr9:12923200-12925400 Enhancers Muscle Satellite Cultured Cells --
16 chr9:12923400-12924800 Enhancers HSMM muscle
17 chr9:12924000-12924400 Flanking Active TSS HSMMtube muscle
18 chr9:12924000-12925400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
19 chr9:12924000-12931000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
20 chr9:12924200-12925200 Weak transcription Rectal Smooth Muscle rectum
21 chr9:12924200-12928000 Weak transcription Adipose Nuclei Adipose

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