| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:79505545-79505596 | Rare:13 | ||||
| chr16:79598953-79598957 | Rare:1 | ||||
| chr16:81696353-81696603 | Common:2; Rare:65 | ||||
| chr16:84607813-84607995 | Common:2; Rare:43 | ||||
| chr16:87956356-87956539 | Common:1; Rare:51 | ||||
| chr16:88100904-88100938 | Common:1; Rare:8 | ||||
| chr16:89052955-89053121 | Rare:48 | ||||
| chr17:5500029-5500315 | Common:3; Rare:54 | ||||
| chr17:6657200-6657354 | Common:3; Rare:22 | ||||
| chr17:7887535-7887796 | Rare:58 | ||||
| chr17:7915918-7916088 | Common:3; Rare:67 | ||||
| chr17:16438672-16439064 | Common:1; Rare:97 | ||||
| chr17:16439401-16439506 | Common:2; Rare:38 | ||||
| chr17:17216270-17216395 | Common:2; Rare:33; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:19306175-19306362 | Rare:42 |