| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2245436-2245821 | Common:1; Rare:131 | ||||
| chr6:2971515-2971964 | Common:3; Rare:113 | ||||
| chr6:3118595-3118737 | Common:2; Rare:46 | ||||
| chr6:3157539-3157633 | Common:6; Rare:40 | ||||
| chr6:4021213-4021422 | Rare:96 | ||||
| chr6:5003644-5003834 | Common:5; Rare:59 | ||||
| chr6:5260729-5260988 | Common:2; Rare:78; Clinvar (benign):2 | ||||
| chr6:8435360-8435659 | Common:4; Rare:105 | ||||
| chr6:10694614-10694994 | Common:4; Rare:99 | ||||
| chr6:10747582-10747881 | Common:3; Rare:111 | ||||
| chr6:11232633-11232893 | Rare:54 | ||||
| chr6:13615170-13615538 | Common:2; Rare:148 | ||||
| chr6:16761454-16761726 | Common:2; Rare:84 | ||||
| chr6:17600211-17600355 | Common:2; Rare:48 | ||||
| chr6:24666858-24667210 | Common:3; Rare:143 |