| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:77190725-77190985 | Common:9; Rare:85 | ||||
| chr16:77191133-77191224 | Common:1; Rare:40 | ||||
| chr16:81006884-81007192 | Common:3; Rare:91 | ||||
| chr16:82170174-82170310 | Common:3; Rare:74 | ||||
| chr16:84116806-84117066 | Common:3; Rare:103 | ||||
| chr16:84145095-84145284 | Common:1; Rare:94; Clinvar:1 | ||||
| chr16:84504641-84504841 | Common:4; Rare:83 | ||||
| chr16:85027636-85027801 | Common:1; Rare:84 | ||||
| chr16:85613094-85613354 | Common:1; Rare:98 | ||||
| chr16:85799312-85799764 | Common:3; Rare:140 | ||||
| chr16:86555182-86555287 | Rare:53 | ||||
| chr16:87765945-87766055 | Common:1; Rare:41 | ||||
| chr16:88570159-88570416 | Common:2; Rare:91 | ||||
| chr16:88663070-88663362 | Common:7; Rare:119 | ||||
| chr16:88856878-88857143 | Common:4; Rare:122; Clinvar:2; Clinvar (benign):2 |