| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49788576-49788759 | Common:1; Rare:61 | ||||
| chr17:50095052-50095427 | Common:2; Rare:117 | ||||
| chr17:50188972-50189258 | Rare:66; Clinvar:2 | ||||
| chr17:50194177-50194376 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr17:50345926-50346140 | Common:4; Rare:71 | ||||
| chr17:50372909-50373250 | Common:3; Rare:119 | ||||
| chr17:50384907-50385121 | Common:2; Rare:37 | ||||
| chr17:50719444-50719667 | Common:1; Rare:89 | ||||
| chr17:50866351-50866636 | Common:3; Rare:84 | ||||
| chr17:51079470-51079650 | Common:1; Rare:40 | ||||
| chr17:51153292-51153657 | Common:1; Rare:95 | ||||
| chr17:51166124-51166579 | Common:3; Rare:96 | ||||
| chr17:51260312-51260611 | Common:3; Rare:129 | ||||
| chr17:52159555-52159635 | Rare:23 | ||||
| chr17:52159961-52160023 | Rare:11 |