| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22973509-22973909 | Rare:143 | ||||
| chr14:22980650-22981030 | Common:4; Rare:139 | ||||
| chr14:23364004-23364460 | Common:2; Rare:164 | ||||
| chr14:23364500-23364930 | Common:1; Rare:89 | ||||
| chr14:23436860-23437220 | Common:1; Rare:88 | ||||
| chr14:23438621-23439057 | Common:4; Rare:146 | ||||
| chr14:23631970-23632270 | Common:3; Rare:69 | ||||
| chr14:23660260-23660521 | Common:3; Rare:65 | ||||
| chr14:23670530-23670830 | Common:2; Rare:63 | ||||
| chr14:23694388-23695177 | Common:11; Rare:266 | ||||
| chr14:24079805-24080085 | Common:2; Rare:52 | ||||
| chr14:24080997-24081238 | Common:2; Rare:70; Clinvar:4; Clinvar (benign):2 | ||||
| chr14:24196244-24196588 | Rare:65 | ||||
| chr14:25152252-25152652 | Common:3; Rare:104 | ||||
| chr14:25607152-25607552 | Common:3; Rare:138 |