| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:2227546-2228109 | Common:4; Rare:541 | ||||
| chr1:2311190-2311840 | Common:4; Rare:193 | ||||
| chr1:2314740-2315190 | Common:3; Rare:131 | ||||
| chr1:2441690-2442070 | Common:3; Rare:74 | ||||
| chr1:2475048-2475305 | Common:2; Rare:55 | ||||
| chr1:2534762-2535162 | Common:9; Rare:139 | ||||
| chr1:2546005-2546523 | Common:17; Rare:424 | ||||
| chr1:2546836-2547220 | Common:6; Rare:194 | ||||
| chr1:2548709-2549109 | Common:9; Rare:140 | ||||
| chr1:2578352-2578538 | Common:2; Rare:41 | ||||
| chr1:2583933-2584125 | Common:2; Rare:55 | ||||
| chr1:2643129-2643390 | Common:2; Rare:195 | ||||
| chr1:3132660-3132946 | Common:4; Rare:95 | ||||
| chr1:3186401-3186850 | Common:8; Rare:304; Clinvar:3; Clinvar (benign):4 | ||||
| chr1:3359709-3360010 | Common:6; Rare:170 |