| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:71130527-71130682 | Rare:61; Clinvar:2 | ||||
| chr3:71306000-71306195 | Common:2; Rare:33 | ||||
| chr3:71360720-71360910 | Common:2; Rare:28 | ||||
| chr3:71582002-71582332 | Rare:92 | ||||
| chr3:87227201-87227323 | Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058914-88059313 | Common:3; Rare:151 | ||||
| chr3:88149617-88150000 | Rare:99 | ||||
| chr3:94062910-94063090 | Rare:40 | ||||
| chr3:97764492-97764594 | Rare:15 | ||||
| chr3:97972395-97972607 | Common:4; Rare:59 | ||||
| chr3:99817569-99817938 | Rare:113 | ||||
| chr3:100260708-100261027 | Rare:85 | ||||
| chr3:100334658-100334786 | Common:1; Rare:57 | ||||
| chr3:100401378-100401539 | Common:1; Rare:38 | ||||
| chr3:100709194-100709392 | Common:4; Rare:70 |