| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:110204890-110205179 | Common:5; Rare:287; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:110212252-110212658 | Common:6; Rare:210 | ||||
| chr2:110212710-110213000 | Rare:47 | ||||
| chr2:110675226-110675626 | Common:1; Rare:117 | ||||
| chr2:110677952-110678363 | Common:4; Rare:567 | ||||
| chr2:110678479-110678879 | Rare:79 | ||||
| chr2:110732350-110732680 | Common:2; Rare:169 | ||||
| chr2:110732610-110733112 | Common:7; Rare:202 | ||||
| chr2:111120440-111120610 | Common:2; Rare:61 | ||||
| chr2:111120547-111121028 | Common:21; Rare:855 | ||||
| chr2:111121811-111122751 | Common:16; Rare:896 | ||||
| chr2:111883536-111883936 | Common:11; Rare:188 | ||||
| chr2:111884036-111884610 | Common:13; Rare:567 | ||||
| chr2:111898272-111898672 | Common:10; Rare:395 | ||||
| chr2:112054710-112055000 | Common:1; Rare:12 |