Variant report

Variant rs7524589
Chromosome Location chr1:155611784-155611785
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:155595000-155613000 Weak transcription Osteobl bone
2 chr1:155605000-155618000 Weak transcription Placenta Amnion Placenta Amnion
3 chr1:155605400-155613000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr1:155606400-155613000 Weak transcription HSMM muscle
5 chr1:155607400-155612000 Weak transcription HSMMtube muscle
6 chr1:155607400-155612800 Weak transcription Muscle Satellite Cultured Cells --
7 chr1:155607400-155621200 Weak transcription Duodenum Smooth Muscle Duodenum
8 chr1:155607600-155613200 Weak transcription A549 lung
9 chr1:155608000-155613000 Weak transcription NH-A brain
10 chr1:155609400-155611800 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr1:155609400-155611800 Enhancers HepG2 liver
12 chr1:155610400-155614000 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr1:155610600-155614200 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:155611200-155613800 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
15 chr1:155611400-155611800 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
16 chr1:155611400-155611800 Enhancers Adipose Nuclei Adipose
17 chr1:155611600-155611800 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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