| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:13615204-13615515 | Common:2; Rare:129 | ||||
| chr6:13814021-13814250 | Common:3; Rare:59 | ||||
| chr6:14117540-14117783 | Common:1; Rare:86 | ||||
| chr6:16761450-16761728 | Common:2; Rare:85 | ||||
| chr6:17600276-17600401 | Common:2; Rare:42 | ||||
| chr6:17706736-17707040 | Common:1; Rare:81 | ||||
| chr6:18122613-18122763 | Common:1; Rare:35; Clinvar (benign):2 | ||||
| chr6:24495013-24495267 | Common:1; Rare:98; Clinvar:13; Clinvar (benign):7 | ||||
| chr6:24666735-24667146 | Common:3; Rare:190 | ||||
| chr6:24775256-24775534 | Rare:68 | ||||
| chr6:26056318-26056546 | Common:4; Rare:160 | ||||
| chr6:26123736-26124409 | Common:7; Rare:337 | ||||
| chr6:26156297-26156760 | Common:3; Rare:340 | ||||
| chr6:26157887-26158169 | Common:4; Rare:106 | ||||
| chr6:26189078-26189315 | Common:5; Rare:85 |