| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31180535-31180870 | Common:3; Rare:126 | ||||
| chr16:31442618-31442846 | Common:2; Rare:42 | ||||
| chr16:31442962-31443225 | Common:1; Rare:59 | ||||
| chr16:31458177-31458377 | Common:1; Rare:60 | ||||
| chr16:31458791-31459241 | Common:2; Rare:127 | ||||
| chr16:31459264-31459575 | Common:2; Rare:126 | ||||
| chr16:31459652-31460100 | Common:1; Rare:213 | ||||
| chr16:31471901-31471963 | Rare:11 | ||||
| chr16:31472084-31472198 | Rare:32 | ||||
| chr16:31472405-31472511 | Rare:25 | ||||
| chr16:31484641-31484833 | Rare:68; Clinvar (pathogenic):1 | ||||
| chr16:31484842-31484864 | Rare:9 | ||||
| chr16:31484906-31485126 | Rare:55; Clinvar (pathogenic):1 | ||||
| chr16:31487681-31487789 | Common:1; Rare:31; Clinvar (pathogenic):1 | ||||
| chr16:31507612-31507850 | Common:2; Rare:60 |