| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89088027-89088544 | Common:5; Rare:125 | ||||
| chr15:89243725-89244216 | Common:2; Rare:136; Clinvar:3 | ||||
| chr15:89244400-89244483 | Rare:19 | ||||
| chr15:89334516-89334613 | Rare:32 | ||||
| chr15:89334693-89335121 | Common:4; Rare:180; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:89575085-89575565 | Common:6; Rare:139 | ||||
| chr15:89655377-89655608 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr15:89690660-89690818 | Common:2; Rare:47 | ||||
| chr15:89691133-89691191 | Rare:8 | ||||
| chr15:89750706-89751050 | Common:5; Rare:150 | ||||
| chr15:89760555-89760637 | Common:3; Rare:16 | ||||
| chr15:89776546-89776683 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:89893698-89893754 | Rare:7 | ||||
| chr15:89893868-89894195 | Common:4; Rare:101 | ||||
| chr15:89894231-89894393 | Rare:46 |