| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:126084097-126084189 | Common:1; Rare:32 | ||||
| chr3:127598136-127598458 | Common:3; Rare:90 | ||||
| chr3:128153383-128153491 | Rare:31 | ||||
| chr3:128879429-128879675 | Common:4; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183793-129184074 | Common:2; Rare:95 | ||||
| chr3:129439846-129440139 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893594-129893882 | Rare:127 | ||||
| chr3:130893919-130894231 | Common:3; Rare:91 | ||||
| chr3:131381472-131381805 | Common:2; Rare:84 | ||||
| chr3:131502876-131503052 | Common:1; Rare:67 | ||||
| chr3:132659785-132660022 | Common:3; Rare:51 | ||||
| chr3:133661896-133661989 | Rare:23 | ||||
| chr3:134485701-134485727 | Rare:12 | ||||
| chr3:134485953-134486145 | Common:2; Rare:64 | ||||
| chr3:136862030-136862275 | Common:1; Rare:69 |