Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:12613260-12613720 | Common:28; Rare:470 | ||||
chr16:12613690-12614070 | Common:16; Rare:355 | ||||
chr16:14364560-14364900 | Common:3; Rare:75 | ||||
chr16:14399529-14399857 | Common:1; Rare:58 | ||||
chr16:14401642-14401933 | Common:2; Rare:55 | ||||
chr16:14405630-14405910 | Rare:85 | ||||
chr16:14486659-14486826 | Rare:41 | ||||
chr16:15154713-15155020 | Common:10; Rare:301 | ||||
chr16:20598782-20599090 | Common:11; Rare:125 | ||||
chr16:20803610-20804057 | Common:1; Rare:144 | ||||
chr16:21116363-21116488 | Rare:19 | ||||
chr16:21260950-21261510 | Common:6; Rare:139; Clinvar (benign):2 | ||||
chr16:21520176-21520583 | Common:7; Rare:132 | ||||
chr16:21995001-21995209 | Rare:78 | ||||
chr16:24844683-24844809 | Common:1; Rare:20 |