Variant report

Variant rs1316434
Chromosome Location chr6:133916028-133916029
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:133912400-133925200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr6:133912600-133916800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr6:133913000-133916800 Weak transcription NHLF lung
4 chr6:133913400-133917400 Enhancers Fetal Lung lung
5 chr6:133913600-133916200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr6:133913800-133917000 Enhancers Fetal Stomach stomach
7 chr6:133915200-133917400 Enhancers Muscle Satellite Cultured Cells --
8 chr6:133915200-133917400 Enhancers A549 lung
9 chr6:133915400-133917000 Enhancers Osteobl bone
10 chr6:133915600-133917000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr6:133915800-133916200 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr6:133915800-133916400 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr6:133915800-133916400 Enhancers NHDF-Ad bronchial
14 chr6:133915800-133917000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr6:133915800-133917200 Enhancers Hela-S3 cervix
16 chr6:133916000-133916200 Active TSS Ovary ovary
17 chr6:133916000-133925200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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