Variant report

Variant rs531640941
Chromosome Location chr6:133912963-133912964
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:133910400-133913400 Weak transcription Fetal Lung lung
2 chr6:133911200-133914000 Enhancers HMEC breast
3 chr6:133911400-133913800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr6:133911400-133913800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr6:133911600-133913600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr6:133911600-133914000 Enhancers Muscle Satellite Cultured Cells --
7 chr6:133911800-133913000 Flanking Active TSS A549 lung
8 chr6:133911800-133913000 Enhancers NHLF lung
9 chr6:133912000-133913600 Enhancers NHEK skin
10 chr6:133912000-133913800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr6:133912000-133913800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr6:133912400-133913800 Weak transcription Fetal Stomach stomach
13 chr6:133912400-133915800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr6:133912400-133925200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr6:133912600-133913600 Enhancers Osteobl bone
16 chr6:133912600-133915400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
17 chr6:133912600-133916800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
18 chr6:133912800-133913200 Weak transcription Hela-S3 cervix
19 chr6:133912800-133913800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
20 chr6:133912800-133915800 Weak transcription NHDF-Ad bronchial

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