| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34007550-34007940 | Common:5; Rare:220; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:34007976-34008272 | Common:5; Rare:196; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:34655930-34656410 | Common:6; Rare:190 | ||||
| chr5:34915191-34915355 | Rare:82 | ||||
| chr5:34915458-34915775 | Common:2; Rare:166 | ||||
| chr5:34929237-34929725 | Common:4; Rare:261 | ||||
| chr5:34929804-34929982 | Rare:95 | ||||
| chr5:35617530-35617950 | Common:2; Rare:127 | ||||
| chr5:36151816-36152229 | Rare:224 | ||||
| chr5:36240854-36241160 | Common:1; Rare:115 | ||||
| chr5:36241514-36242387 | Common:11; Rare:380; Clinvar:1; Clinvar (benign):8 | ||||
| chr5:36301825-36302251 | Common:5; Rare:111 | ||||
| chr5:36606467-36606640 | Rare:30 | ||||
| chr5:36876625-36877006 | Common:2; Rare:181; Clinvar:3; Clinvar (benign):4 | ||||
| chr5:36877014-36877161 | Rare:49; Clinvar:1 |