| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88663084-88663377 | Common:8; Rare:121 | ||||
| chr16:88706406-88706556 | Common:2; Rare:72 | ||||
| chr16:88856917-88857180 | Common:4; Rare:125; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217619-89217749 | Common:1; Rare:61 | ||||
| chr16:89508262-89508463 | Common:2; Rare:117; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560541-89560749 | Rare:91 | ||||
| chr16:89657647-89658107 | Common:3; Rare:240 | ||||
| chr16:89686634-89686704 | Common:5; Rare:44 | ||||
| chr16:89720865-89720999 | Common:1; Rare:35 | ||||
| chr16:89873482-89873785 | Common:2; Rare:139 | ||||
| chr16:89972468-89972621 | Common:1; Rare:51 | ||||
| chr16:90019376-90019681 | Common:6; Rare:92 | ||||
| chr17:331117-331193 | Common:2; Rare:16 | ||||
| chr17:714792-714899 | Common:2; Rare:36 | ||||
| chr17:752222-752347 | Common:2; Rare:46 |