| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102784686-102785086 | Common:2; Rare:114 | ||||
| chr14:102784990-102785290 | Common:2; Rare:59 | ||||
| chr14:102785240-102785610 | Common:1; Rare:104 | ||||
| chr14:102799650-102800200 | Common:4; Rare:115 | ||||
| chr14:102802480-102802988 | Common:1; Rare:210 | ||||
| chr14:102804749-102805768 | Common:8; Rare:336 | ||||
| chr14:102806070-102806470 | Common:3; Rare:95 | ||||
| chr14:102806760-102806998 | Common:3; Rare:89 | ||||
| chr14:102807482-102808196 | Common:1; Rare:282 | ||||
| chr14:102818115-102818515 | Common:4; Rare:92 | ||||
| chr14:102819240-102819820 | Common:3; Rare:127 | ||||
| chr14:102819821-102820102 | Common:2; Rare:107 | ||||
| chr14:102841258-102841585 | Common:2; Rare:63 | ||||
| chr14:102849297-102849697 | Common:1; Rare:110 | ||||
| chr14:102869851-102870495 | Common:2; Rare:281; Clinvar:2; Clinvar (benign):2 |