| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52194398-52194504 | Rare:32 | ||||
| chr13:52617322-52617541 | Common:1; Rare:54 | ||||
| chr13:57629927-57630166 | Common:1; Rare:71 | ||||
| chr13:87671227-87671427 | Common:1; Rare:57 | ||||
| chr13:87673121-87673224 | Common:1; Rare:23 | ||||
| chr13:97432940-97433274 | Common:4; Rare:98 | ||||
| chr13:99015956-99016279 | Rare:53 | ||||
| chr13:107868357-107868412 | Rare:17 | ||||
| chr14:23512958-23513378 | Common:2; Rare:91 | ||||
| chr14:28764362-28764566 | Common:1; Rare:46 | ||||
| chr14:28766547-28766768 | Common:2; Rare:68 | ||||
| chr14:28768233-28768394 | Rare:38; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:28768409-28768486 | Rare:20; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:28774530-28774820 | Common:3; Rare:49 | ||||
| chr14:32203267-32203549 | Common:11; Rare:116 |