| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51583983-51584057 | Common:1; Rare:22 | ||||
| chr13:51584256-51584624 | Common:4; Rare:110 | ||||
| chr13:51584887-51585023 | Common:1; Rare:28 | ||||
| chr13:51803675-51804392 | Common:2; Rare:205 | ||||
| chr13:52012058-52012491 | Common:2; Rare:164; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:52128319-52128636 | Common:1; Rare:55 | ||||
| chr13:52156866-52157228 | Common:1; Rare:62 | ||||
| chr13:52159395-52159509 | Common:2; Rare:48 | ||||
| chr13:52159533-52159707 | Common:1; Rare:36 | ||||
| chr13:52450050-52450342 | Common:2; Rare:61 | ||||
| chr13:52450346-52450395 | Rare:9 | ||||
| chr13:52450536-52450856 | Common:1; Rare:89 | ||||
| chr13:52455096-52455170 | Common:2; Rare:16 | ||||
| chr13:52455267-52455582 | Common:3; Rare:119 | ||||
| chr13:52652206-52652482 | Common:3; Rare:81 |