| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:2044908-2045046 | Common:1; Rare:36 | ||||
| chr8:6406496-6406702 | Common:3; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708142-6708435 | Common:3; Rare:133 | ||||
| chr8:6709042-6709238 | Common:2; Rare:81 | ||||
| chr8:8386384-8386783 | Common:4; Rare:133 | ||||
| chr8:8386810-8387210 | Common:1; Rare:101 | ||||
| chr8:8893526-8893775 | Common:3; Rare:103 | ||||
| chr8:9002719-9002993 | Common:4; Rare:132 | ||||
| chr8:9555567-9555959 | Common:7; Rare:143 | ||||
| chr8:10054539-10054891 | Common:2; Rare:188 | ||||
| chr8:10839748-10840130 | Common:4; Rare:142 | ||||
| chr8:11201329-11201570 | Common:3; Rare:80 | ||||
| chr8:11201801-11201913 | Rare:30 | ||||
| chr8:11284321-11284536 | Common:2; Rare:82 | ||||
| chr8:11467586-11467899 | Rare:100 |