Variant report

Variant rs9389087
Chromosome Location chr6:133908231-133908232
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:133898600-133911400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr6:133904800-133909800 Enhancers Fetal Lung lung
3 chr6:133906000-133908800 Weak transcription HSMM muscle
4 chr6:133906000-133912000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr6:133907200-133911400 Weak transcription Fetal Kidney kidney
6 chr6:133907800-133908400 Weak transcription HSMMtube muscle
7 chr6:133908000-133908400 Enhancers Fetal Stomach stomach
8 chr6:133908000-133908600 ZNF genes & repeats A549 lung
9 chr6:133908000-133908800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr6:133908000-133909600 Enhancers NHDF-Ad bronchial
11 chr6:133908200-133908600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr6:133908200-133908600 Enhancers NHLF lung
13 chr6:133908200-133909800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr6:133908200-133909800 Enhancers Osteobl bone
15 chr6:133908200-133911800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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