| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:11795771-11796010 | Common:3; Rare:135 | ||||
| chr8:11802438-11802835 | Common:6; Rare:219 | ||||
| chr8:11808319-11808666 | Common:6; Rare:170 | ||||
| chr8:11808752-11808846 | Common:1; Rare:58 | ||||
| chr8:11867981-11868298 | Common:1; Rare:145 | ||||
| chr8:12754088-12754184 | Rare:31 | ||||
| chr8:13133212-13133572 | Common:14; Rare:102 | ||||
| chr8:13566770-13566905 | Common:5; Rare:52 | ||||
| chr8:15540182-15540441 | Common:4; Rare:98; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:16186252-16186379 | Common:1; Rare:29 | ||||
| chr8:17246583-17247063 | Common:5; Rare:199 | ||||
| chr8:17800849-17801074 | Common:3; Rare:58 | ||||
| chr8:17801075-17801358 | Common:7; Rare:107 | ||||
| chr8:17922616-17923021 | Common:5; Rare:160 | ||||
| chr8:18084800-18085046 | Common:2; Rare:74; Clinvar (benign):1 |