| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:56918299-56918755 | Common:3; Rare:176 | ||||
| chr15:57706960-57707070 | Common:2; Rare:51 | ||||
| chr15:58332018-58332294 | Common:3; Rare:51 | ||||
| chr15:58749529-58750089 | Common:4; Rare:189 | ||||
| chr15:58770975-58771328 | Common:3; Rare:138 | ||||
| chr15:58933437-58933766 | Common:2; Rare:131 | ||||
| chr15:58988045-58988150 | Common:1; Rare:33 | ||||
| chr15:59372545-59372694 | Common:1; Rare:38 | ||||
| chr15:59372778-59373035 | Common:2; Rare:88 | ||||
| chr15:60397901-60398168 | Common:2; Rare:66 | ||||
| chr15:60479060-60479207 | Common:2; Rare:61 | ||||
| chr15:62060349-62060525 | Rare:69 | ||||
| chr15:62390344-62390633 | Common:2; Rare:138 | ||||
| chr15:63042353-63042966 | Common:8; Rare:192; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr15:63157145-63157292 | Rare:25 |