| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1771494-1771848 | Common:3; Rare:141 | ||||
| chr16:1827161-1827232 | Common:1; Rare:33 | ||||
| chr16:1943193-1943497 | Common:1; Rare:89 | ||||
| chr16:1959373-1959696 | Common:6; Rare:132 | ||||
| chr16:1971874-1972090 | Common:3; Rare:64 | ||||
| chr16:2047804-2048058 | Rare:127; Clinvar:2; Clinvar (benign):5 | ||||
| chr16:2102526-2102818 | Common:6; Rare:136; Clinvar:2; Clinvar (benign):6 | ||||
| chr16:2474983-2475151 | Rare:53 | ||||
| chr16:2682360-2682628 | Rare:124 | ||||
| chr16:2752549-2752851 | Common:2; Rare:128 | ||||
| chr16:2770329-2770360 | Common:1; Rare:7 | ||||
| chr16:2777023-2777371 | Common:2; Rare:122 | ||||
| chr16:2911775-2912051 | Common:5; Rare:93 | ||||
| chr16:3112533-3112619 | Common:2; Rare:18 | ||||
| chr16:3134852-3135162 | Common:3; Rare:86 |