| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:79505545-79505596 | Not yet | Rare:13 | 58 | ||
| chr16:79598953-79598957 | Not yet | Rare:1 | 1 | ||
| chr16:81696353-81696603 | Not yet | Common:2; Rare:65 | 194 | ||
| chr16:84607813-84607995 | Not yet | Common:2; Rare:43 | 162 | ||
| chr16:87956356-87956539 | Not yet | Common:1; Rare:51 | 221 | ||
| chr16:88100904-88100938 | Not yet | Common:1; Rare:8 | 29 | ||
| chr16:89052955-89053121 | Not yet | Rare:48 | 204 | ||
| chr17:5500029-5500315 | Not yet | Common:3; Rare:54 | 201 | ||
| chr17:6657200-6657354 | Not yet | Common:3; Rare:22 | 124 | ||
| chr17:7887535-7887796 | Not yet | Rare:58 | 188 | ||
| chr17:7915918-7916088 | Not yet | Common:3; Rare:67 | 122 | ||
| chr17:16438672-16439064 | Not yet | Common:1; Rare:97 | 299 | ||
| chr17:16439401-16439506 | Not yet | Common:2; Rare:38 | 68 | ||
| chr17:17216270-17216395 | Not yet | Common:2; Rare:33; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | 117 | ||
| chr17:19306175-19306362 | Not yet | Rare:42 | 144 |