Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:267988-268113 | Common:1; Rare:51 | ||||
chr18:596736-597055 | Common:21; Rare:154 | ||||
chr18:658279-658414 | Common:1; Rare:25 | ||||
chr18:812135-812484 | Common:4; Rare:133 | ||||
chr18:812498-812635 | Common:1; Rare:38 | ||||
chr18:812741-812794 | Rare:18 | ||||
chr18:812852-812918 | Rare:16 | ||||
chr18:2571413-2571593 | Rare:57 | ||||
chr18:2655553-2655740 | Common:3; Rare:90 | ||||
chr18:2655832-2655999 | Common:1; Rare:52 | ||||
chr18:3013078-3013378 | Common:3; Rare:108 | ||||
chr18:3247247-3247908 | Common:4; Rare:192 | ||||
chr18:3261820-3262236 | Common:6; Rare:131 | ||||
chr18:3449327-3449745 | Common:2; Rare:101 | ||||
chr18:3450063-3450478 | Common:2; Rare:120; Clinvar (benign):2 |