| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74507231-74508681 | Common:11; Rare:1054 | ||||
| chr2:74528870-74529453 | Common:14; Rare:648; Clinvar (benign):2 | ||||
| chr2:74529571-74530074 | Rare:854; Clinvar:26; Clinvar (benign):7 | ||||
| chr2:74530454-74531040 | Common:7; Rare:429; Clinvar:15; Clinvar (benign):2 | ||||
| chr2:74548416-74549270 | Common:3; Rare:606 | ||||
| chr2:74552925-74553325 | Common:2; Rare:85 | ||||
| chr2:74553716-74554813 | Common:16; Rare:1073 | ||||
| chr2:74554727-74555372 | Common:6; Rare:464 | ||||
| chr2:74555304-74555991 | Common:5; Rare:345 | ||||
| chr2:74576840-74577240 | Rare:65 | ||||
| chr2:74653989-74654389 | Common:8; Rare:389 | ||||
| chr2:74833796-74834196 | Common:2; Rare:450 | ||||
| chr2:74834653-74835642 | Common:13; Rare:824 | ||||
| chr2:74958042-74958442 | Common:4; Rare:125 | ||||
| chr2:74958403-74958803 | Common:25; Rare:513 |