| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:970428-970620 | Rare:55 | ||||
| chr16:970746-970999 | Common:1; Rare:113 | ||||
| chr16:1308553-1308723 | Common:5; Rare:44 | ||||
| chr16:1308768-1308915 | Common:3; Rare:54 | ||||
| chr16:1308990-1309183 | Rare:46 | ||||
| chr16:1309332-1309776 | Rare:159 | ||||
| chr16:1309850-1309950 | Rare:30 | ||||
| chr16:1310043-1310274 | Common:1; Rare:85 | ||||
| chr16:1351729-1352020 | Common:2; Rare:137; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1379056-1379259 | Rare:55 | ||||
| chr16:1379545-1379715 | Common:1; Rare:71 | ||||
| chr16:1414588-1414927 | Common:6; Rare:105 | ||||
| chr16:1420643-1421082 | Common:3; Rare:169 | ||||
| chr16:1421097-1421318 | Common:6; Rare:51 | ||||
| chr16:1474156-1474353 | Common:2; Rare:58 |