| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69522856-69522975 | Rare:23 | ||||
| chr16:69990414-69990566 | Common:6; Rare:32 | ||||
| chr16:70042931-70042993 | Rare:8 | ||||
| chr16:70065563-70065706 | Common:2; Rare:34 | ||||
| chr16:70065772-70065981 | Common:1; Rare:77 | ||||
| chr16:70066410-70066577 | Common:1; Rare:33 | ||||
| chr16:70153193-70153567 | Common:2; Rare:94 | ||||
| chr16:70188274-70188352 | Common:4; Rare:11 | ||||
| chr16:70254681-70254864 | Common:1; Rare:58; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:70332800-70333117 | Rare:85 | ||||
| chr16:70726477-70726681 | Common:1; Rare:34 | ||||
| chr16:70742783-70742897 | Common:1; Rare:24 | ||||
| chr16:71326043-71326178 | Common:1; Rare:25 | ||||
| chr16:71513744-71513909 | Rare:36 | ||||
| chr16:71707487-71707648 | Rare:36 |