| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88856831-88857153 | Common:4; Rare:151; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89217627-89217710 | Common:1; Rare:33 | ||||
| chr16:89657632-89657827 | Common:1; Rare:99 | ||||
| chr16:89816646-89816788 | Common:2; Rare:65; Clinvar:1 | ||||
| chr16:89923150-89923345 | Rare:74 | ||||
| chr16:89972521-89972614 | Rare:30 | ||||
| chr16:90022555-90022691 | Rare:52 | ||||
| chr17:714792-714982 | Common:3; Rare:60 | ||||
| chr17:752276-752379 | Common:1; Rare:30 | ||||
| chr17:1516628-1516954 | Common:1; Rare:115 | ||||
| chr17:1684795-1685070 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1716245-1716576 | Common:4; Rare:101 | ||||
| chr17:1829832-1830042 | Common:7; Rare:88 | ||||
| chr17:2303496-2303610 | Rare:43 | ||||
| chr17:2303734-2303980 | Common:2; Rare:94 |