| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49022009-49022158 | Rare:48; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49028290-49028491 | Rare:63 | ||||
| chr3:49029264-49029349 | Rare:29 | ||||
| chr3:49029352-49029737 | Common:2; Rare:211 | ||||
| chr3:49104687-49105109 | Common:1; Rare:146; Clinvar:1; Clinvar (benign):6 | ||||
| chr3:49276956-49277112 | Common:1; Rare:53 | ||||
| chr3:49339994-49340125 | Common:2; Rare:63 | ||||
| chr3:49411820-49412445 | Common:2; Rare:215 | ||||
| chr3:49469986-49470325 | Common:1; Rare:105 | ||||
| chr3:49674228-49674412 | Common:1; Rare:73 | ||||
| chr3:49689460-49689605 | Rare:45 | ||||
| chr3:49723834-49724214 | Common:9; Rare:123 | ||||
| chr3:49856513-49856704 | Common:2; Rare:52 | ||||
| chr3:49903831-49903988 | Rare:49 | ||||
| chr3:50173814-50174114 | Rare:96 |