| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:20900889-20901098 | Common:2; Rare:46 | ||||
| chr16:21158550-21158718 | Common:1; Rare:50 | ||||
| chr16:21599364-21599716 | Common:4; Rare:125 | ||||
| chr16:21952975-21953419 | Common:1; Rare:111; Clinvar (benign):3 | ||||
| chr16:22374593-22374835 | Common:1; Rare:79 | ||||
| chr16:22436961-22437326 | Rare:127 | ||||
| chr16:22437350-22437388 | Rare:5 | ||||
| chr16:22437418-22437498 | Rare:25 | ||||
| chr16:22437505-22437690 | Common:2; Rare:46 | ||||
| chr16:22814739-22814976 | Rare:89 | ||||
| chr16:23453127-23453250 | Rare:35 | ||||
| chr16:23510415-23510557 | Common:4; Rare:70 | ||||
| chr16:23557320-23557639 | Common:3; Rare:110; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23596164-23596334 | Common:1; Rare:62 | ||||
| chr16:23641219-23641530 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 |