Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7687440-7687556 | Rare:28; Clinvar:2 | ||||
chr17:7854880-7855180 | Common:1; Rare:119 | ||||
chr17:7855183-7855708 | Common:4; Rare:215 | ||||
chr17:7857100-7857296 | Common:1; Rare:95 | ||||
chr17:7857382-7857711 | Common:3; Rare:107 | ||||
chr17:7885187-7885350 | Rare:51 | ||||
chr17:7885493-7885656 | Rare:32 | ||||
chr17:7931869-7932258 | Common:5; Rare:104 | ||||
chr17:8151174-8151491 | Common:3; Rare:80 | ||||
chr17:8162926-8163081 | Rare:46 | ||||
chr17:8176313-8176459 | Rare:48 | ||||
chr17:8210541-8210720 | Common:2; Rare:36 | ||||
chr17:8248042-8248181 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
chr17:8249180-8249337 | Common:1; Rare:47 | ||||
chr17:8295341-8295538 | Common:1; Rare:50 |