Variant report

Variant rs6898190
Chromosome Location chr5:127914867-127914868
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:127910600-127915400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr5:127913800-127915800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr5:127914000-127915200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr5:127914000-127915600 Enhancers Placenta Amnion Placenta Amnion
5 chr5:127914000-127915800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr5:127914000-127916000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr5:127914000-127916000 Enhancers HMEC breast
8 chr5:127914000-127916000 Enhancers NHEK skin
9 chr5:127914200-127915600 Flanking Active TSS A549 lung
10 chr5:127914400-127915800 Enhancers HSMM muscle
11 chr5:127914400-127915800 Enhancers Osteobl bone
12 chr5:127914400-127916200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr5:127914600-127915000 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr5:127914600-127915400 Weak transcription NH-A brain
15 chr5:127914600-127922600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
16 chr5:127914800-127915200 Enhancers Muscle Satellite Cultured Cells --
17 chr5:127914800-127915200 Weak transcription Placenta Placenta
18 chr5:127914800-127915400 Enhancers Hela-S3 cervix

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