| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:52679238-52679785 | Common:5; Rare:123 | ||||
| chr15:52790311-52790537 | Common:1; Rare:84 | ||||
| chr15:55195936-55196181 | Common:2; Rare:53 | ||||
| chr15:55196481-55196737 | Common:1; Rare:65 | ||||
| chr15:55196811-55197333 | Common:8; Rare:173 | ||||
| chr15:55289016-55289308 | Common:3; Rare:60 | ||||
| chr15:55289515-55289976 | Common:5; Rare:115 | ||||
| chr15:55290099-55290370 | Common:2; Rare:61 | ||||
| chr15:55318640-55318773 | Common:1; Rare:36 | ||||
| chr15:55318795-55319308 | Common:5; Rare:144 | ||||
| chr15:55319329-55319509 | Rare:52 | ||||
| chr15:55407716-55407956 | Common:3; Rare:51 | ||||
| chr15:55407996-55408763 | Common:7; Rare:193 | ||||
| chr15:55498144-55498531 | Common:8; Rare:164; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:55587610-55587768 | Rare:54 |