| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:62390418-62390576 | Rare:91 | ||||
| chr15:63042543-63043440 | Common:5; Rare:233; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr15:63048257-63048719 | Common:5; Rare:175; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63049231-63049459 | Common:1; Rare:55 | ||||
| chr15:63054271-63054536 | Common:2; Rare:47 | ||||
| chr15:63054727-63054852 | Common:1; Rare:20 | ||||
| chr15:63062900-63063128 | Common:1; Rare:42 | ||||
| chr15:63063324-63063533 | Common:2; Rare:33 | ||||
| chr15:63063863-63063984 | Common:1; Rare:26 | ||||
| chr15:63064016-63064078 | Rare:24; Clinvar:2; Clinvar (benign):3 | ||||
| chr15:63121684-63121894 | Common:1; Rare:61 | ||||
| chr15:63122379-63122705 | Common:4; Rare:100 | ||||
| chr15:63157095-63157244 | Rare:26 | ||||
| chr15:63157341-63157526 | Common:2; Rare:77 | ||||
| chr15:63157966-63158162 | Common:3; Rare:46 |