| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:155314452-155314764 | Common:9; Rare:111 | ||||
| chr6:157323486-157323625 | Common:2; Rare:52 | ||||
| chr6:158168205-158168388 | Common:2; Rare:63 | ||||
| chr6:158644670-158644957 | Common:3; Rare:113 | ||||
| chr6:158818161-158818266 | Common:1; Rare:33 | ||||
| chr6:158819316-158819457 | Common:2; Rare:52 | ||||
| chr6:158999754-158999886 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159000130-159000329 | Common:1; Rare:49 | ||||
| chr6:159693233-159693594 | Common:5; Rare:102 | ||||
| chr6:159726917-159727162 | Common:1; Rare:94 | ||||
| chr6:159727360-159727637 | Common:5; Rare:122 | ||||
| chr6:159789538-159790004 | Common:4; Rare:155 | ||||
| chr6:159790272-159790559 | Common:8; Rare:104 | ||||
| chr6:162727766-162727974 | Rare:55; Clinvar:1 | ||||
| chr6:166342505-166342653 | Common:3; Rare:58 |