| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:80060537-80060582 | Rare:6 | ||||
| chr15:80060652-80060705 | Rare:11 | ||||
| chr15:80060917-80061042 | Common:1; Rare:28 | ||||
| chr15:80152397-80152916 | Common:10; Rare:50; Clinvar (benign):1 | ||||
| chr15:80152958-80153085 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:80153393-80153484 | Common:1; Rare:14 | ||||
| chr15:80404272-80404409 | Rare:40 | ||||
| chr15:80404916-80404953 | Rare:4 | ||||
| chr15:80694891-80695409 | Common:4; Rare:160 | ||||
| chr15:80695700-80696004 | Rare:71 | ||||
| chr15:80779088-80779380 | Common:2; Rare:71 | ||||
| chr15:80989165-80989379 | Common:3; Rare:55 | ||||
| chr15:80989563-80989641 | Rare:20 | ||||
| chr15:80989676-80990136 | Common:5; Rare:191 | ||||
| chr15:81324090-81324531 | Common:6; Rare:123 |