| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121650005-121650163 | Rare:79 | ||||
| chr2:121736813-121737105 | Common:8; Rare:202 | ||||
| chr2:121755368-121755786 | Common:11; Rare:260 | ||||
| chr2:127294046-127294258 | Common:4; Rare:144; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:127387120-127387560 | Common:12; Rare:211 | ||||
| chr2:127387875-127388285 | Common:20; Rare:337 | ||||
| chr2:127418332-127418499 | Common:3; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:127526351-127526626 | Common:4; Rare:184 | ||||
| chr2:127526760-127527070 | Common:2; Rare:101 | ||||
| chr2:127811149-127811320 | Common:2; Rare:115 | ||||
| chr2:127858082-127858335 | Common:8; Rare:202 | ||||
| chr2:127886148-127886492 | Common:2; Rare:163 | ||||
| chr2:128027227-128027585 | Common:2; Rare:265 | ||||
| chr2:128091043-128091382 | Common:16; Rare:216 | ||||
| chr2:128318809-128318997 | Common:7; Rare:153 |