| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:95961794-95962085 | Common:1; Rare:67 | ||||
| chr5:96433139-96434269 | Common:4; Rare:250; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:96661887-96662099 | Common:2; Rare:37 | ||||
| chr5:96662830-96663140 | Common:1; Rare:82 | ||||
| chr5:96702688-96702815 | Common:1; Rare:45 | ||||
| chr5:96702960-96703300 | Common:5; Rare:72 | ||||
| chr5:96807376-96807482 | Rare:25 | ||||
| chr5:96807920-96808101 | Rare:43 | ||||
| chr5:96808348-96808565 | Common:1; Rare:45 | ||||
| chr5:96934697-96934982 | Common:1; Rare:83 | ||||
| chr5:96935235-96935396 | Common:1; Rare:47 | ||||
| chr5:96935803-96936134 | Common:10; Rare:111 | ||||
| chr5:97142600-97142903 | Common:3; Rare:69 | ||||
| chr5:97183168-97183536 | Common:4; Rare:135 | ||||
| chr5:97183633-97183901 | Common:1; Rare:64 |