| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:94545665-94546008 | Common:8; Rare:188 | ||||
| chr10:95561362-95561579 | Common:6; Rare:115 | ||||
| chr10:95656595-95656913 | Common:2; Rare:175; Clinvar:12; Clinvar (benign):4 | ||||
| chr10:95693842-95694055 | Common:2; Rare:89; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95907706-95907940 | Common:4; Rare:103 | ||||
| chr10:96043394-96043614 | Common:1; Rare:127 | ||||
| chr10:96129760-96130110 | Common:3; Rare:144 | ||||
| chr10:96130110-96130880 | Common:6; Rare:462 | ||||
| chr10:96576450-96577151 | Common:10; Rare:201 | ||||
| chr10:96586359-96586787 | Common:5; Rare:202 | ||||
| chr10:96586777-96587138 | Common:8; Rare:260 | ||||
| chr10:96587300-96587680 | Common:3; Rare:87 | ||||
| chr10:96831983-96832324 | Rare:181 | ||||
| chr10:96832490-96832750 | Common:4; Rare:176 | ||||
| chr10:96832845-96833055 | Common:2; Rare:67 |