Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:99107546-99107767 | Common:1; Rare:45 | ||||
chr15:99138977-99138989 | Rare:4 | ||||
chr15:99210345-99210527 | Common:1; Rare:34 | ||||
chr16:1172145-1172311 | Common:3; Rare:56 | ||||
chr16:1200464-1200806 | Common:4; Rare:181; Clinvar:2; Clinvar (benign):10 | ||||
chr16:1205910-1206192 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):5 | ||||
chr16:1228903-1229320 | Common:19; Rare:63 | ||||
chr16:2603353-2603473 | Rare:52 | ||||
chr16:2673351-2673683 | Common:10; Rare:113 | ||||
chr16:3022914-3023273 | Common:1; Rare:104 | ||||
chr16:4307585-4307783 | Common:3; Rare:71 | ||||
chr16:4899376-4899415 | Rare:16 | ||||
chr16:15041067-15041169 | Rare:33 | ||||
chr16:15710457-15710576 | Common:3; Rare:36 | ||||
chr16:15747872-15748189 | Common:6; Rare:89; Clinvar:9; Clinvar (benign):10 |