| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:106194286-106194597 | Common:4; Rare:116 | ||||
| chr2:108449073-108449274 | Rare:84 | ||||
| chr2:108534163-108534461 | Common:7; Rare:122 | ||||
| chr2:108719359-108719586 | Common:3; Rare:98; Clinvar (benign):2 | ||||
| chr2:110204961-110205067 | Rare:48; Clinvar:1 | ||||
| chr2:110677997-110678258 | Rare:88 | ||||
| chr2:111884121-111884303 | Common:1; Rare:57 | ||||
| chr2:112255009-112255146 | Common:1; Rare:59 | ||||
| chr2:112275392-112275642 | Common:1; Rare:86 | ||||
| chr2:112542148-112542489 | Common:1; Rare:106 | ||||
| chr2:112584378-112584510 | Common:1; Rare:25 | ||||
| chr2:112584527-112584645 | Rare:39 | ||||
| chr2:112645718-112645953 | Common:1; Rare:87 | ||||
| chr2:112764584-112764843 | Common:2; Rare:83; Clinvar (pathogenic):1 | ||||
| chr2:113173852-113174013 | Common:1; Rare:31 |