| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:11868018-11868158 | Rare:69 | ||||
| chr8:15540192-15540406 | Common:4; Rare:79; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:17237368-17237463 | Rare:28 | ||||
| chr8:17246059-17246373 | Common:5; Rare:109 | ||||
| chr8:17246591-17247042 | Common:5; Rare:193 | ||||
| chr8:17801056-17801345 | Common:7; Rare:104 | ||||
| chr8:17922606-17923028 | Common:5; Rare:169 | ||||
| chr8:17923103-17923185 | Rare:21 | ||||
| chr8:18084931-18085046 | Rare:24 | ||||
| chr8:19013500-19014051 | Common:8; Rare:190 | ||||
| chr8:19313358-19313765 | Common:3; Rare:126 | ||||
| chr8:19601813-19602056 | Common:2; Rare:63 | ||||
| chr8:19602153-19602269 | Common:1; Rare:25 | ||||
| chr8:19642017-19642307 | Common:1; Rare:57 | ||||
| chr8:19757669-19757964 | Common:6; Rare:63 |