| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41968740-41969020 | Rare:56 | ||||
| chr15:41968964-41969880 | Common:17; Rare:335 | ||||
| chr15:41970005-41970400 | Common:6; Rare:145 | ||||
| chr15:41970565-41971223 | Common:4; Rare:173 | ||||
| chr15:41971382-41971863 | Common:1; Rare:139 | ||||
| chr15:41993120-41993390 | Common:1; Rare:38 | ||||
| chr15:42009552-42009789 | Common:3; Rare:45 | ||||
| chr15:42010478-42010832 | Common:8; Rare:109 | ||||
| chr15:42033418-42033699 | Common:2; Rare:35 | ||||
| chr15:42035430-42035750 | Common:1; Rare:125 | ||||
| chr15:42065038-42065438 | Common:2; Rare:88 | ||||
| chr15:42191978-42192566 | Common:5; Rare:206 | ||||
| chr15:42275210-42275758 | Common:12; Rare:174 | ||||
| chr15:42401678-42401855 | Rare:64; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
| chr15:42493728-42494128 | Common:3; Rare:96 |