| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80220269-80220527 | Common:2; Rare:87; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80220737-80221042 | Common:2; Rare:71 | ||||
| chr17:80260310-80260988 | Common:12; Rare:127 | ||||
| chr17:80261014-80261066 | Rare:12 | ||||
| chr17:80261291-80261637 | Common:3; Rare:83 | ||||
| chr17:80414831-80415266 | Common:3; Rare:226 | ||||
| chr17:80415325-80415500 | Common:4; Rare:64 | ||||
| chr17:80415603-80415798 | Common:2; Rare:88 | ||||
| chr17:80476581-80476693 | Rare:30 | ||||
| chr17:80544744-80544909 | Common:2; Rare:41 | ||||
| chr17:80545231-80545260 | Rare:7 | ||||
| chr17:80991411-80991714 | Rare:52 | ||||
| chr17:80991794-80991992 | Common:1; Rare:70 | ||||
| chr17:80992196-80992278 | Common:1; Rare:26 | ||||
| chr17:81034647-81034701 | Rare:16 |