Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24232837-24232934 | Rare:23 | ||||
chr14:24235493-24235770 | Common:3; Rare:57 | ||||
chr14:24242258-24242433 | Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24242562-24242774 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24271453-24271620 | Common:1; Rare:50 | ||||
chr14:24299706-24299917 | Common:5; Rare:70 | ||||
chr14:24310011-24310058 | Rare:7 | ||||
chr14:24429855-24429996 | Common:1; Rare:33 | ||||
chr14:24442659-24443043 | Common:5; Rare:121 | ||||
chr14:25049901-25050208 | Common:2; Rare:96 | ||||
chr14:30622190-30622350 | Rare:57 | ||||
chr14:31100988-31101144 | Rare:38 | ||||
chr14:31207107-31207189 | Rare:22 | ||||
chr14:31207463-31207854 | Common:2; Rare:130 | ||||
chr14:31208137-31208237 | Common:1; Rare:27 |