Variant report

Variant rs6741773
Chromosome Location chr2:99738962-99738963
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:99718000-99740200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr2:99718600-99739600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr2:99723800-99739600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr2:99729400-99741600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr2:99735600-99741400 Weak transcription Brain Angular Gyrus brain
6 chr2:99736400-99742200 Weak transcription Pancreas Pancrea
7 chr2:99738000-99742000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:99738200-99742200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr2:99738600-99742000 Weak transcription Primary T helper naive cells from peripheral blood blood
10 chr2:99738800-99743800 Weak transcription HepG2 liver

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