| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231528605-231528741 | Common:1; Rare:54 | ||||
| chr1:234373284-234373682 | Common:1; Rare:178; Clinvar (benign):5 | ||||
| chr1:235504385-235504703 | Common:5; Rare:97 | ||||
| chr1:240091734-240091950 | Common:3; Rare:88 | ||||
| chr1:243255241-243255386 | Common:1; Rare:32 | ||||
| chr1:243255741-243256132 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:246566136-246566612 | Common:3; Rare:159 | ||||
| chr1:246724247-246724489 | Common:2; Rare:96 | ||||
| chr10:988325-988498 | Common:1; Rare:74 | ||||
| chr10:1048874-1049095 | Common:2; Rare:114 | ||||
| chr10:1049343-1049534 | Common:6; Rare:87 | ||||
| chr10:5813395-5813480 | Common:2; Rare:45 | ||||
| chr10:7787940-7788253 | Common:1; Rare:132 | ||||
| chr10:12195797-12196238 | Rare:117 | ||||
| chr10:13099784-13100222 | Common:4; Rare:107; Clinvar:3; Clinvar (benign):5 |