| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48413059-48413178 | Rare:17 | ||||
| chr13:52194386-52194510 | Rare:38 | ||||
| chr13:52617322-52617541 | Common:1; Rare:54 | ||||
| chr13:57629940-57630125 | Common:1; Rare:49 | ||||
| chr13:76885086-76885123 | Rare:13 | ||||
| chr13:87671072-87671392 | Common:1; Rare:85 | ||||
| chr13:99087946-99087966 | Rare:4 | ||||
| chr13:102394493-102394646 | Common:1; Rare:58 | ||||
| chr13:110174462-110174715 | Rare:84; Clinvar (benign):3 | ||||
| chr13:110424793-110424996 | Common:4; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:113828580-113828826 | Common:2; Rare:85 | ||||
| chr14:32203265-32203650 | Common:13; Rare:165 | ||||
| chr14:34874146-34874224 | Common:1; Rare:22 | ||||
| chr14:41604902-41604995 | Common:2; Rare:17 | ||||
| chr14:49633956-49634043 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 |