| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121755415-121755786 | Common:5; Rare:123 | ||||
| chr2:127294063-127294196 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387904-127388255 | Common:9; Rare:156 | ||||
| chr2:127609668-127610015 | Common:1; Rare:100 | ||||
| chr2:127619950-127620038 | Rare:17 | ||||
| chr2:127620371-127620611 | Common:3; Rare:72 | ||||
| chr2:127811121-127811259 | Rare:45 | ||||
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:127885878-127885991 | Rare:29 | ||||
| chr2:128091102-128091343 | Common:5; Rare:75 | ||||
| chr2:128187261-128187537 | Rare:55 | ||||
| chr2:130181553-130181700 | Common:1; Rare:49 | ||||
| chr2:130182087-130182387 | Common:2; Rare:114 | ||||
| chr2:130342127-130342296 | Rare:65 | ||||
| chr2:130342645-130342930 | Common:5; Rare:89 |