| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:181243692-181243951 | Common:4; Rare:96 | ||||
| chr5:181261083-181261262 | Rare:60 | ||||
| chr6:291974-292128 | Common:1; Rare:31 | ||||
| chr6:292417-292550 | Rare:41 | ||||
| chr6:292624-292996 | Common:6; Rare:50 | ||||
| chr6:693066-693198 | Rare:41 | ||||
| chr6:2245595-2245821 | Rare:73 | ||||
| chr6:2765082-2765438 | Common:8; Rare:148 | ||||
| chr6:2841838-2842122 | Common:3; Rare:52 | ||||
| chr6:3118577-3118741 | Common:2; Rare:53 | ||||
| chr6:4021216-4021414 | Rare:90 | ||||
| chr6:5003609-5003821 | Common:6; Rare:63 | ||||
| chr6:5004016-5004160 | Common:1; Rare:59 | ||||
| chr6:5260685-5261051 | Common:5; Rare:129; Clinvar (benign):4 | ||||
| chr6:6588404-6588805 | Common:3; Rare:98 |