Variant report

Variant rs11953201
Chromosome Location chr5:127910560-127910561
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:127907200-127910600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
2 chr5:127907400-127911000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chr5:127907800-127911000 Enhancers A549 lung
4 chr5:127908000-127910600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr5:127908400-127910800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr5:127908800-127910800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr5:127908800-127910800 Enhancers Placenta Placenta
8 chr5:127908800-127910800 Enhancers Placenta Amnion Placenta Amnion
9 chr5:127908800-127911000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr5:127908800-127914200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr5:127910200-127914000 Weak transcription Muscle Satellite Cultured Cells --
12 chr5:127910200-127914400 Weak transcription NH-A brain
13 chr5:127910400-127913800 Weak transcription Hela-S3 cervix
14 chr5:127910400-127914000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr5:127910400-127914000 Weak transcription HMEC breast
16 chr5:127910400-127914000 Weak transcription NHEK skin

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