| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105398036-105398666 | Common:20; Rare:617 | ||||
| chr14:105398613-105399013 | Common:1; Rare:176 | ||||
| chr14:105419250-105419580 | Common:1; Rare:51 | ||||
| chr14:105419630-105420100 | Common:4; Rare:552 | ||||
| chr14:105474610-105474850 | Common:1; Rare:76 | ||||
| chr14:105485821-105486221 | Common:6; Rare:126 | ||||
| chr14:105489841-105490066 | Common:3; Rare:74 | ||||
| chr14:105490060-105490203 | Common:4; Rare:105 | ||||
| chr14:105490194-105491376 | Common:9; Rare:1018 | ||||
| chr15:22785900-22786860 | Common:16; Rare:980; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr15:22838356-22838833 | Common:19; Rare:901 | ||||
| chr15:22838900-22839645 | Common:6; Rare:217 | ||||
| chr15:22980030-22980874 | Common:16; Rare:623 | ||||
| chr15:23039387-23039868 | Common:7; Rare:670 | ||||
| chr15:23565368-23565823 | Common:9; Rare:487 |