Variant report

Variant rs58407167
Chromosome Location chr9:98472783-98472784
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:98470600-98473200 Enhancers Fetal Stomach stomach
2 chr9:98471200-98474800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr9:98472000-98474000 Enhancers Fetal Intestine Small intestine
4 chr9:98472400-98474000 Enhancers Fetal Intestine Large intestine
5 chr9:98472600-98472800 Enhancers Fetal Muscle Trunk muscle
6 chr9:98472600-98472800 Flanking Bivalent TSS/Enh HepG2 liver

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