| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29995601-29995708 | Rare:47 | ||||
| chr16:29996073-29996329 | Common:2; Rare:94 | ||||
| chr16:30010960-30011137 | Rare:44 | ||||
| chr16:30030801-30030890 | Rare:10 | ||||
| chr16:30053038-30053163 | Common:1; Rare:44 | ||||
| chr16:30064277-30064430 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr16:30065102-30065115 | Rare:4 | ||||
| chr16:30065560-30065841 | Rare:99 | ||||
| chr16:30075889-30076045 | Rare:51 | ||||
| chr16:30122928-30123371 | Common:8; Rare:125 | ||||
| chr16:30183510-30183629 | Common:1; Rare:30 | ||||
| chr16:30355199-30355438 | Common:1; Rare:81 | ||||
| chr16:30407475-30407635 | Rare:55 | ||||
| chr16:30445863-30445955 | Rare:31 | ||||
| chr16:30534814-30535110 | Common:3; Rare:94 |