Variant report

Variant rs7718877
Chromosome Location chr5:117895033-117895034
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:117892600-117895200 Enhancers HMEC breast
2 chr5:117892600-117896000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr5:117892800-117895200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr5:117893000-117895200 Enhancers NHDF-Ad bronchial
5 chr5:117893200-117895600 Weak transcription Left Ventricle heart
6 chr5:117894400-117895800 Weak transcription Fetal Lung lung
7 chr5:117894600-117895600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr5:117894600-117897800 Active TSS Right Atrium heart
9 chr5:117894800-117896800 Enhancers Fetal Heart heart
10 chr5:117895000-117896400 Enhancers Fetal Adrenal Gland Adrenal Gland

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