| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:240025297-240025579 | Common:2; Rare:115; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:240605315-240605464 | Common:1; Rare:29 | ||||
| chr2:241272802-241273016 | Rare:78 | ||||
| chr2:241315122-241315398 | Common:5; Rare:90 | ||||
| chr2:241315650-241315978 | Common:5; Rare:127 | ||||
| chr2:241508535-241508872 | Common:2; Rare:105 | ||||
| chr2:241701877-241702068 | Common:1; Rare:78 | ||||
| chr20:380955-381065 | Common:1; Rare:29 | ||||
| chr20:1118468-1118655 | Common:3; Rare:56 | ||||
| chr20:2652420-2652648 | Common:7; Rare:80 | ||||
| chr20:2840672-2840724 | Rare:16 | ||||
| chr20:3209447-3209508 | Rare:15 | ||||
| chr20:4686268-4686483 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr20:5112883-5113182 | Common:1; Rare:116 | ||||
| chr20:5950414-5950696 | Common:8; Rare:86 |