| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:959238-959363 | Not yet | Common:1; Rare:76 | 171 | ||
| chr1:1231916-1232320 | Not yet | Rare:151; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | 322 | ||
| chr1:1307888-1307971 | Not yet | Rare:16 | 104 | ||
| chr1:1324594-1324802 | Not yet | Common:2; Rare:115 | 258 | ||
| chr1:1358514-1358982 | Not yet | Common:3; Rare:143 | 334 | ||
| chr1:1399307-1399590 | Not yet | Common:1; Rare:125 | 286 | ||
| chr1:1407213-1407410 | Not yet | Common:1; Rare:90 | 228 | ||
| chr1:1435556-1435746 | Not yet | Rare:70 | 127 | ||
| chr1:1574495-1574963 | Not yet | Common:1; Rare:200 | 348 | ||
| chr1:1658920-1659032 | Not yet | Common:2; Rare:42 | 229 | ||
| chr1:1724286-1724508 | Not yet | Common:4; Rare:78 | 358 | ||
| chr1:2207244-2207369 | Not yet | Rare:36 | 150 | ||
| chr1:2391510-2391953 | Not yet | Common:2; Rare:154 | 316 | ||
| chr1:3624741-3625052 | Not yet | Common:1; Rare:103 | 297 | ||
| chr1:3857179-3857521 | Not yet | Common:1; Rare:91 | 350 |