| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69013140-69013540 | Common:11; Rare:150 | ||||
| chr2:69387198-69387442 | Rare:76; Clinvar:2 | ||||
| chr2:69437352-69437584 | Rare:113; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:69643012-69643412 | Common:2; Rare:118 | ||||
| chr2:69643611-69644072 | Common:1; Rare:136 | ||||
| chr2:69741399-69742355 | Common:7; Rare:257 | ||||
| chr2:69829429-69829743 | Common:1; Rare:122 | ||||
| chr2:69893866-69894004 | Rare:38 | ||||
| chr2:70086873-70087120 | Common:1; Rare:117 | ||||
| chr2:70087310-70087491 | Common:2; Rare:66 | ||||
| chr2:70190641-70190811 | Rare:45 | ||||
| chr2:70190979-70191209 | Common:2; Rare:62 | ||||
| chr2:70248228-70248405 | Rare:60 | ||||
| chr2:70248481-70248814 | Common:5; Rare:131 | ||||
| chr2:70257921-70258209 | Common:2; Rare:96 |