| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:57244974-57245379 | Common:3; Rare:134 | ||||
| chr16:57447354-57447517 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57646766-57646983 | Common:3; Rare:36 | ||||
| chr16:57668151-57668389 | Common:2; Rare:54 | ||||
| chr16:57984965-57985202 | Common:5; Rare:78 | ||||
| chr16:57999554-57999756 | Rare:41 | ||||
| chr16:58000526-58000785 | Common:2; Rare:62 | ||||
| chr16:58001295-58001458 | Rare:47 | ||||
| chr16:58129238-58129575 | Common:3; Rare:105 | ||||
| chr16:58392813-58392898 | Common:1; Rare:21 | ||||
| chr16:58515408-58515547 | Common:2; Rare:55 | ||||
| chr16:58525307-58525603 | Common:2; Rare:59 | ||||
| chr16:58629772-58630112 | Common:2; Rare:90 | ||||
| chr16:58684711-58684833 | Rare:37 | ||||
| chr16:65121873-65122202 | Common:1; Rare:119 |