| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8152348-8152695 | Common:4; Rare:84 | ||||
| chr17:8162873-8163108 | Common:1; Rare:85 | ||||
| chr17:8176304-8176497 | Rare:60 | ||||
| chr17:8247555-8247625 | Common:1; Rare:21 | ||||
| chr17:8248018-8248190 | Common:3; Rare:73; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:8249195-8249331 | Common:1; Rare:42 | ||||
| chr17:8435696-8436034 | Common:4; Rare:130 | ||||
| chr17:8630878-8631162 | Common:3; Rare:98 | ||||
| chr17:10026209-10026489 | Common:1; Rare:46 | ||||
| chr17:10697460-10697654 | Common:3; Rare:90; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:11598949-11599148 | Common:2; Rare:56 | ||||
| chr17:11997382-11997631 | Common:3; Rare:98 | ||||
| chr17:13017662-13017802 | Common:1; Rare:63; Clinvar (benign):3 | ||||
| chr17:13017957-13018240 | Common:4; Rare:82; Clinvar (benign):2 | ||||
| chr17:14069342-14069599 | Common:2; Rare:93; Clinvar:4; Clinvar (benign):3 |