| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:124025139-124025434 | Common:3; Rare:91 | ||||
| chr2:127294077-127294261 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387918-127388285 | Common:9; Rare:162 | ||||
| chr2:127526411-127526607 | Common:2; Rare:71 | ||||
| chr2:127811129-127811327 | Common:1; Rare:70 | ||||
| chr2:127858050-127858341 | Common:4; Rare:117 | ||||
| chr2:127885886-127886305 | Common:1; Rare:112 | ||||
| chr2:128028029-128028249 | Common:1; Rare:63 | ||||
| chr2:128091030-128091378 | Common:8; Rare:111 | ||||
| chr2:130181528-130181797 | Common:4; Rare:120 | ||||
| chr2:130182101-130182442 | Common:2; Rare:124 | ||||
| chr2:130342104-130342295 | Rare:81; Clinvar:1 | ||||
| chr2:130342642-130342935 | Common:5; Rare:92 | ||||
| chr2:130756087-130756344 | Common:2; Rare:89 | ||||
| chr2:131093382-131093571 | Common:1; Rare:87 |