| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185395885-185396063 | Common:1; Rare:55 | ||||
| chr4:185396430-185396935 | Rare:177 | ||||
| chr4:185397029-185397293 | Rare:98 | ||||
| chr4:185425957-185426240 | Common:1; Rare:73 | ||||
| chr4:186191491-186191832 | Common:5; Rare:116; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723821-186723906 | Common:1; Rare:25 | ||||
| chr4:186726681-186726730 | Common:1; Rare:18 | ||||
| chr4:189940609-189941133 | Common:19; Rare:197 | ||||
| chr5:218097-218349 | Common:3; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:443074-443288 | Common:10; Rare:99 | ||||
| chr5:612147-612357 | Rare:82 | ||||
| chr5:891201-891609 | Common:2; Rare:124 | ||||
| chr5:892489-893006 | Common:5; Rare:169 | ||||
| chr5:1326678-1326794 | Common:8; Rare:13 | ||||
| chr5:1345037-1345275 | Common:2; Rare:88 |