| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:8501536-8501863 | Common:1; Rare:115 | ||||
| chr3:9362952-9363098 | Common:2; Rare:54 | ||||
| chr3:9792391-9792570 | Rare:49 | ||||
| chr3:9792777-9793119 | Common:3; Rare:119 | ||||
| chr3:10026329-10026465 | Rare:40 | ||||
| chr3:12288897-12289075 | Common:1; Rare:36 | ||||
| chr3:12664064-12664324 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:13480040-13480330 | Common:2; Rare:67 | ||||
| chr3:14124728-14125144 | Common:4; Rare:117; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178573-14178858 | Common:2; Rare:147; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:14947401-14947549 | Common:2; Rare:71 | ||||
| chr3:15427490-15427629 | Common:1; Rare:48 | ||||
| chr3:15601512-15601756 | Common:4; Rare:100 | ||||
| chr3:16264881-16265220 | Common:2; Rare:109 | ||||
| chr3:19946994-19947138 | Common:2; Rare:50 |