| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:110115808-110115953 | Common:2; Rare:33 | ||||
| chr2:112764594-112764859 | Common:2; Rare:87; Clinvar (pathogenic):1 | ||||
| chr2:113627065-113627257 | Common:1; Rare:57 | ||||
| chr2:113756610-113756791 | Common:3; Rare:71 | ||||
| chr2:119366811-119367059 | Common:1; Rare:72 | ||||
| chr2:119678960-119679216 | Common:5; Rare:69 | ||||
| chr2:120012927-120013080 | Common:2; Rare:62 | ||||
| chr2:121530607-121530880 | Common:7; Rare:109 | ||||
| chr2:121649431-121649650 | Common:2; Rare:65 | ||||
| chr2:127526442-127526612 | Common:1; Rare:51 | ||||
| chr2:127811139-127811258 | Rare:37 | ||||
| chr2:130181561-130181737 | Common:2; Rare:72 | ||||
| chr2:130342132-130342279 | Rare:58 | ||||
| chr2:131105193-131105367 | Common:1; Rare:79 | ||||
| chr2:131492772-131493107 | Common:8; Rare:106 |