| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:11769568-11769798 | Common:5; Rare:100 | ||||
| chr8:11795866-11796010 | Rare:71 | ||||
| chr8:11802414-11802810 | Common:7; Rare:224 | ||||
| chr8:11868003-11868263 | Rare:123 | ||||
| chr8:12194059-12194296 | Common:3; Rare:51 | ||||
| chr8:12754078-12754186 | Common:1; Rare:39 | ||||
| chr8:15417420-15417520 | Rare:14 | ||||
| chr8:15540175-15540441 | Common:4; Rare:99; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:17246589-17247108 | Common:5; Rare:209 | ||||
| chr8:17247151-17247293 | Rare:57; Clinvar (benign):1 | ||||
| chr8:17801092-17801298 | Common:6; Rare:79 | ||||
| chr8:17922606-17923006 | Common:5; Rare:156 | ||||
| chr8:18084787-18084864 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr8:18084915-18085030 | Common:1; Rare:26 | ||||
| chr8:19013637-19013976 | Common:5; Rare:96 |