Variant report

Variant rs4467667
Chromosome Location chr5:180101599-180101600
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:180100600-180101600 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
2 chr5:180100800-180101600 Bivalent/Poised TSS Fetal Brain Female brain
3 chr5:180100800-180101600 Bivalent Enhancer Fetal Stomach stomach
4 chr5:180101400-180101600 Bivalent Enhancer Primary T cells fromperipheralblood blood
5 chr5:180101400-180101600 Enhancers Primary T helper naive cells fromperipheralblood blood
6 chr5:180101400-180101600 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
7 chr5:180101400-180101600 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr5:180101400-180101600 Bivalent Enhancer Fetal Thymus thymus

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