| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15945158-15945297 | Common:2; Rare:38 | ||||
| chr17:15999533-15999843 | Common:2; Rare:153; Clinvar:4; Clinvar (benign):5 | ||||
| chr17:16214972-16215089 | Rare:36 | ||||
| chr17:16215451-16215729 | Common:2; Rare:126 | ||||
| chr17:16217058-16217250 | Rare:55; Clinvar:1 | ||||
| chr17:16353418-16353560 | Rare:49 | ||||
| chr17:16381002-16381162 | Common:2; Rare:75 | ||||
| chr17:16492090-16492510 | Common:5; Rare:128 | ||||
| chr17:16569120-16569399 | Common:1; Rare:81 | ||||
| chr17:16653752-16653986 | Rare:65 | ||||
| chr17:17042221-17042523 | Common:19; Rare:115 | ||||
| chr17:17237141-17237456 | Common:4; Rare:93; Clinvar (benign):2 | ||||
| chr17:17280690-17280958 | Common:4; Rare:113 | ||||
| chr17:17281289-17281434 | Common:1; Rare:38 | ||||
| chr17:17281511-17282167 | Common:6; Rare:131 |