| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121530589-121530880 | Common:7; Rare:115 | ||||
| chr2:121649418-121649715 | Common:2; Rare:85 | ||||
| chr2:121650082-121650132 | Rare:12 | ||||
| chr2:121736846-121737099 | Common:4; Rare:90 | ||||
| chr2:127294096-127294219 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387958-127388250 | Common:7; Rare:128 | ||||
| chr2:127526410-127526519 | Common:2; Rare:53 | ||||
| chr2:127811121-127811504 | Common:3; Rare:117 | ||||
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:127885876-127886479 | Common:2; Rare:157 | ||||
| chr2:128091156-128091354 | Common:2; Rare:62 | ||||
| chr2:130181553-130181770 | Common:2; Rare:97 | ||||
| chr2:130182094-130182381 | Common:2; Rare:110 | ||||
| chr2:130182448-130182718 | Common:3; Rare:92 | ||||
| chr2:130342111-130342281 | Rare:72; Clinvar:1 |