| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91836415-91836640 | Common:9; Rare:37 | ||||
| chr14:91946956-91947131 | Common:1; Rare:22 | ||||
| chr14:91947390-91947620 | Common:2; Rare:46; Clinvar:1 | ||||
| chr14:92040008-92040148 | Common:3; Rare:43; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92121655-92121990 | Common:5; Rare:110 | ||||
| chr14:92704639-92704780 | Common:2; Rare:47; Clinvar:1 | ||||
| chr14:92793999-92794382 | Rare:120 | ||||
| chr14:93184845-93185013 | Rare:56 | ||||
| chr14:93206985-93207316 | Common:3; Rare:166 | ||||
| chr14:94081123-94081406 | Common:5; Rare:87 | ||||
| chr14:95157416-95157734 | Common:4; Rare:116 | ||||
| chr14:95157957-95158025 | Common:1; Rare:19 | ||||
| chr14:95534609-95534680 | Rare:19 | ||||
| chr14:95534769-95535011 | Common:3; Rare:65 | ||||
| chr14:96204726-96204850 | Common:1; Rare:34 |