| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46052580-46052908 | Common:2; Rare:88 | ||||
| chr13:46387134-46387262 | Common:1; Rare:27 | ||||
| chr13:46552972-46553213 | Common:2; Rare:86 | ||||
| chr13:46553326-46553427 | Common:2; Rare:29 | ||||
| chr13:46796495-46796782 | Common:3; Rare:75 | ||||
| chr13:46796838-46796990 | Rare:39 | ||||
| chr13:46797011-46797397 | Common:3; Rare:116 | ||||
| chr13:48000971-48001038 | Common:1; Rare:9 | ||||
| chr13:48001202-48001533 | Common:3; Rare:140; Clinvar:4; Clinvar (benign):8 | ||||
| chr13:48001753-48001845 | Rare:25 | ||||
| chr13:48001850-48001944 | Common:1; Rare:30 | ||||
| chr13:48037551-48037829 | Common:2; Rare:123; Clinvar:2 | ||||
| chr13:48037855-48038198 | Common:6; Rare:118 | ||||
| chr13:48094663-48094705 | Common:1; Rare:12 | ||||
| chr13:48094998-48095281 | Common:2; Rare:137 |