| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4806981-4807210 | Common:4; Rare:72 | ||||
| chr17:4833200-4833514 | Rare:91 | ||||
| chr17:4899384-4899570 | Common:2; Rare:104; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:4939906-4940348 | Common:2; Rare:130 | ||||
| chr17:4948932-4949133 | Common:1; Rare:66 | ||||
| chr17:4950970-4951125 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr17:4967767-4967903 | Rare:58 | ||||
| chr17:4969292-4969407 | Rare:39 | ||||
| chr17:4987640-4987753 | Rare:47 | ||||
| chr17:5191835-5192106 | Common:2; Rare:88 | ||||
| chr17:5419624-5419863 | Common:3; Rare:80 | ||||
| chr17:5420144-5420258 | Rare:48 | ||||
| chr17:5486089-5486554 | Common:5; Rare:163 | ||||
| chr17:5486778-5486920 | Common:4; Rare:45 | ||||
| chr17:5501004-5501226 | Common:3; Rare:69 |