| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:77779400-77779840 | Rare:350 | ||||
| chr1:77779804-77780231 | Common:1; Rare:98 | ||||
| chr1:77888130-77889017 | Common:10; Rare:397; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:77926627-77927427 | Common:5; Rare:234; Clinvar:11; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr1:77978306-77978706 | Common:2; Rare:125 | ||||
| chr1:77978762-77979393 | Common:24; Rare:856 | ||||
| chr1:77979380-77979760 | Common:7; Rare:372 | ||||
| chr1:77979896-77980567 | Common:12; Rare:282 | ||||
| chr1:78004200-78005151 | Common:45; Rare:1024 | ||||
| chr1:83998757-83999462 | Common:19; Rare:441 | ||||
| chr1:84077140-84077670 | Common:2; Rare:202 | ||||
| chr1:84077636-84078360 | Common:12; Rare:748 | ||||
| chr1:84298086-84298690 | Common:11; Rare:481 | ||||
| chr1:84298986-84299743 | Common:34; Rare:636 | ||||
| chr1:84299840-84300240 | Common:3; Rare:68 |