| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42422629-42422878 | Rare:104; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr17:42774426-42774680 | Common:3; Rare:44 | ||||
| chr17:42852107-42852124 | Rare:7 | ||||
| chr17:43144834-43144910 | Common:2; Rare:16 | ||||
| chr17:43166269-43166572 | Common:1; Rare:62 | ||||
| chr17:43315653-43315920 | Common:7; Rare:114 | ||||
| chr17:43360973-43361124 | Common:4; Rare:86 | ||||
| chr17:43368082-43368367 | Common:9; Rare:111 | ||||
| chr17:43388294-43388671 | Common:11; Rare:68 | ||||
| chr17:43953183-43953315 | Common:1; Rare:60; Clinvar:1 | ||||
| chr17:44207665-44207984 | Common:1; Rare:101 | ||||
| chr17:44215049-44215125 | Common:2; Rare:18 | ||||
| chr17:44215938-44216089 | Common:2; Rare:37 | ||||
| chr17:45117992-45118373 | Common:2; Rare:128 | ||||
| chr17:45149969-45150171 | Rare:46 |