| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75405590-75405953 | Common:2; Rare:113 | ||||
| chr17:75456351-75456732 | Common:6; Rare:286 | ||||
| chr17:75459470-75459860 | Common:2; Rare:89 | ||||
| chr17:75515396-75515786 | Common:8; Rare:257 | ||||
| chr17:75516331-75516651 | Common:6; Rare:220; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr17:75522750-75523440 | Common:8; Rare:187; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75524610-75525190 | Common:5; Rare:303; Clinvar (benign):1 | ||||
| chr17:75525213-75525858 | Common:15; Rare:485 | ||||
| chr17:75558577-75559567 | Common:29; Rare:506 | ||||
| chr17:75633740-75634186 | Common:4; Rare:240 | ||||
| chr17:75639282-75639721 | Common:2; Rare:165 | ||||
| chr17:75639730-75640200 | Common:5; Rare:246 | ||||
| chr17:75640359-75641068 | Common:6; Rare:244 | ||||
| chr17:75645617-75645872 | Common:3; Rare:54 | ||||
| chr17:75666931-75667515 | Common:16; Rare:391 |