| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34929207-34930050 | Common:9; Rare:884 | ||||
| chr5:34930078-34930478 | Common:7; Rare:90 | ||||
| chr5:35617500-35617983 | Common:8; Rare:471 | ||||
| chr5:36151783-36152209 | Rare:510 | ||||
| chr5:36152443-36152843 | Common:2; Rare:87 | ||||
| chr5:36153354-36153754 | Common:4; Rare:70 | ||||
| chr5:36240702-36241558 | Common:8; Rare:621; Clinvar (benign):1 | ||||
| chr5:36241490-36241913 | Common:11; Rare:408; Clinvar:3; Clinvar (benign):17 | ||||
| chr5:36241880-36242470 | Common:17; Rare:717; Clinvar (benign):8 | ||||
| chr5:36876364-36877021 | Common:8; Rare:705; Clinvar:8; Clinvar (benign):14 | ||||
| chr5:36876960-36877744 | Common:3; Rare:569; Clinvar:7; Clinvar (benign):5 | ||||
| chr5:37370760-37371820 | Common:20; Rare:1116 | ||||
| chr5:37378978-37379802 | Common:6; Rare:423 | ||||
| chr5:38258660-38259160 | Common:2; Rare:142 | ||||
| chr5:38556451-38556951 | Common:15; Rare:714 |