| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10249136-10249202 | Common:3; Rare:16 | ||||
| chr3:10249310-10249590 | Common:1; Rare:108 | ||||
| chr3:10292945-10293136 | Common:1; Rare:43 | ||||
| chr3:10320990-10321286 | Common:2; Rare:115 | ||||
| chr3:11272190-11272511 | Common:4; Rare:78 | ||||
| chr3:11272637-11272723 | Rare:17 | ||||
| chr3:11643050-11643710 | Common:5; Rare:155 | ||||
| chr3:11643873-11644015 | Common:2; Rare:47 | ||||
| chr3:11846630-11847063 | Common:2; Rare:137 | ||||
| chr3:12287718-12287943 | Common:6; Rare:47 | ||||
| chr3:12484267-12484606 | Common:5; Rare:110; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12556849-12557341 | Common:7; Rare:151 | ||||
| chr3:12663860-12663930 | Rare:17; Clinvar:1 | ||||
| chr3:12664050-12664450 | Common:3; Rare:110; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:12840642-12840802 | Common:1; Rare:26 |