| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:181223468-181223759 | Common:4; Rare:76 | ||||
| chr5:181243690-181243979 | Common:4; Rare:102 | ||||
| chr5:181261081-181261262 | Rare:61 | ||||
| chr6:693048-693209 | Rare:51 | ||||
| chr6:2245449-2245821 | Common:1; Rare:128 | ||||
| chr6:2971269-2971679 | Common:5; Rare:105 | ||||
| chr6:3118581-3118743 | Common:2; Rare:54 | ||||
| chr6:3258803-3259058 | Rare:100 | ||||
| chr6:4021174-4021428 | Rare:110 | ||||
| chr6:5003649-5003843 | Common:5; Rare:61 | ||||
| chr6:5004007-5004115 | Common:1; Rare:52 | ||||
| chr6:5260685-5261020 | Common:3; Rare:111; Clinvar (benign):4 | ||||
| chr6:5261265-5261551 | Common:9; Rare:70 | ||||
| chr6:7107553-7107850 | Rare:107 | ||||
| chr6:7313049-7313380 | Common:5; Rare:125 |