| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100376144-100376684 | Common:5; Rare:160 | ||||
| chr14:101761422-101761775 | Common:6; Rare:95 | ||||
| chr14:101809684-101809961 | Rare:58 | ||||
| chr14:101809983-101810177 | Rare:43 | ||||
| chr14:101810221-101810463 | Common:2; Rare:46 | ||||
| chr14:101823754-101824065 | Common:1; Rare:58 | ||||
| chr14:101824281-101824501 | Rare:44 | ||||
| chr14:101825001-101825121 | Rare:21 | ||||
| chr14:101964342-101964642 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102086548-102086647 | Rare:51 | ||||
| chr14:102086946-102087770 | Common:9; Rare:318 | ||||
| chr14:102139150-102139460 | Rare:121 | ||||
| chr14:102139577-102140005 | Rare:145 | ||||
| chr14:102140466-102140616 | Common:1; Rare:36 | ||||
| chr14:102316903-102317090 | Common:4; Rare:74 |