| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127598190-127598446 | Common:3; Rare:69 | ||||
| chr3:127628970-127629227 | Common:1; Rare:86 | ||||
| chr3:127672805-127673028 | Common:4; Rare:109 | ||||
| chr3:127823175-127823340 | Common:3; Rare:32 | ||||
| chr3:128052147-128052562 | Common:3; Rare:139 | ||||
| chr3:128153350-128153496 | Rare:39 | ||||
| chr3:128680633-128680918 | Common:3; Rare:95 | ||||
| chr3:128726077-128726248 | Common:1; Rare:52; Clinvar:3 | ||||
| chr3:128879425-128879694 | Common:4; Rare:135; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129160995-129161139 | Rare:60 | ||||
| chr3:129183764-129184119 | Common:2; Rare:132 | ||||
| chr3:129249512-129249739 | Common:2; Rare:64 | ||||
| chr3:129278777-129278895 | Common:3; Rare:33 | ||||
| chr3:129316233-129316360 | Common:1; Rare:58 | ||||
| chr3:129439823-129440383 | Common:1; Rare:168; Clinvar:2; Clinvar (benign):1 |