| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68265299-68265483 | Rare:28 | ||||
| chr16:68310922-68311133 | Common:2; Rare:102 | ||||
| chr16:68539178-68539379 | Common:1; Rare:91 | ||||
| chr16:69132537-69132688 | Rare:61 | ||||
| chr16:69339548-69339822 | Common:1; Rare:111; Clinvar (benign):1 | ||||
| chr16:69424489-69424682 | Rare:56 | ||||
| chr16:69726448-69726792 | Common:3; Rare:89 | ||||
| chr16:69762288-69762379 | Rare:22 | ||||
| chr16:70114115-70114373 | Common:3; Rare:92 | ||||
| chr16:70346759-70347030 | Common:2; Rare:125 | ||||
| chr16:70523527-70523874 | Common:3; Rare:115; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:71289341-71289697 | Common:3; Rare:118 | ||||
| chr16:71723862-71724052 | Common:4; Rare:65 | ||||
| chr16:71808799-71809155 | Common:1; Rare:144 | ||||
| chr16:71845774-71846023 | Common:2; Rare:75 |