| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5419545-5419882 | Common:3; Rare:118 | ||||
| chr17:5420103-5420227 | Rare:51 | ||||
| chr17:5438854-5439016 | Rare:55 | ||||
| chr17:5486136-5486630 | Common:5; Rare:170 | ||||
| chr17:5486789-5486917 | Common:4; Rare:39 | ||||
| chr17:6640635-6641090 | Common:7; Rare:142 | ||||
| chr17:6651574-6651746 | Common:1; Rare:52 | ||||
| chr17:6755809-6756079 | Common:5; Rare:62 | ||||
| chr17:7012317-7012745 | Rare:137 | ||||
| chr17:7013117-7013486 | Common:1; Rare:101 | ||||
| chr17:7035778-7036076 | Rare:70 | ||||
| chr17:7219728-7219971 | Common:3; Rare:99; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7224366-7224697 | Common:4; Rare:125; Clinvar:10; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
| chr17:7224872-7224894 | Rare:11; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:7234462-7234720 | Common:2; Rare:124 |