Variant report

Variant rs552958004
Chromosome Location chr7:17038077-17038078
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17030000-17038400 Weak transcription Esophagus oesophagus
2 chr7:17031200-17047400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr7:17033400-17052600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr7:17033600-17043400 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr7:17033800-17045200 Weak transcription Placenta Placenta
6 chr7:17037200-17038200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr7:17038000-17038600 Enhancers Fetal Heart heart

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