Variant report

Variant rs59400283
Chromosome Location chr6:145671676-145671677
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145670000-145672000 Enhancers Fetal Heart heart
2 chr6:145670400-145672000 Flanking Active TSS GM12878-XiMat blood
3 chr6:145670800-145671800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr6:145670800-145672800 Enhancers Primary B cells from peripheral blood blood
5 chr6:145671400-145671800 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr6:145671400-145672600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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