Variant report

Variant rs9489184
Chromosome Location chr6:117761268-117761269
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:117760000-117762000 Enhancers Hela-S3 cervix
2 chr6:117760000-117762600 Enhancers HMEC breast
3 chr6:117760400-117761400 ZNF genes & repeats Muscle Satellite Cultured Cells --
4 chr6:117760600-117761400 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr6:117760800-117761400 ZNF genes & repeats NHEK skin
6 chr6:117761000-117762000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr6:117761000-117762600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr6:117761200-117762000 Weak transcription Osteobl bone
9 chr6:117761200-117762200 Weak transcription A549 lung
10 chr6:117761200-117762800 Weak transcription HSMM muscle
11 chr6:117761200-117763400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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