Variant report

Variant rs58524054
Chromosome Location chr1:155612862-155612863
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr1:155607400-155621200 Weak transcription Duodenum Smooth Muscle Duodenum
6 chr1:155607600-155613200 Weak transcription A549 lung
7 chr1:155608000-155613000 Weak transcription NH-A brain
8 chr1:155610400-155614000 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:155610600-155614200 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:155611200-155613800 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
11 chr1:155611800-155613000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr1:155611800-155613000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr1:155612400-155613800 ZNF genes & repeats IMR90 fetal lung fibroblasts Cell Line lung
14 chr1:155612400-155615000 Weak transcription Brain Angular Gyrus brain
15 chr1:155612800-155613200 ZNF genes & repeats Muscle Satellite Cultured Cells --
16 chr1:155612800-155614200 ZNF genes & repeats NHEK skin

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