| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4351257-4351489 | Common:2; Rare:102 | ||||
| chr16:4425773-4425884 | Common:1; Rare:51 | ||||
| chr16:4476273-4476448 | Common:3; Rare:66 | ||||
| chr16:4614871-4615162 | Common:1; Rare:94 | ||||
| chr16:8797631-8797877 | Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:11783019-11783154 | Rare:31 | ||||
| chr16:11851519-11851656 | Rare:65 | ||||
| chr16:11915889-11916277 | Common:2; Rare:159 | ||||
| chr16:14632723-14632995 | Common:1; Rare:92 | ||||
| chr16:14975052-14975167 | Rare:20 | ||||
| chr16:15094251-15094415 | Rare:74 | ||||
| chr16:18790283-18790611 | Common:2; Rare:100 | ||||
| chr16:18801511-18801777 | Common:2; Rare:90 | ||||
| chr16:20806456-20806510 | Rare:20 | ||||
| chr16:23641300-23641530 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):2 |