| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4693437-4693741 | Common:3; Rare:135 | ||||
| chr16:4734142-4734555 | Common:1; Rare:136 | ||||
| chr16:4802573-4802921 | Common:1; Rare:139; Clinvar:8; Clinvar (benign):1 | ||||
| chr16:4847231-4847436 | Common:1; Rare:89 | ||||
| chr16:4870249-4870537 | Common:3; Rare:111 | ||||
| chr16:4891833-4892037 | Common:2; Rare:97 | ||||
| chr16:4937035-4937351 | Common:6; Rare:115 | ||||
| chr16:5033920-5033976 | Rare:23 | ||||
| chr16:5097728-5098007 | Common:4; Rare:102 | ||||
| chr16:8621620-8621745 | Common:1; Rare:46 | ||||
| chr16:8797625-8797900 | Rare:110; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868986-8869267 | Common:4; Rare:126 | ||||
| chr16:9092162-9092249 | Rare:28 | ||||
| chr16:10453521-10453559 | Rare:8 | ||||
| chr16:10580527-10580886 | Common:2; Rare:120 |