| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50328180-50328353 | Rare:49 | ||||
| chr3:50350705-50350894 | Common:1; Rare:28 | ||||
| chr3:50359451-50359569 | Common:2; Rare:35 | ||||
| chr3:50365139-50365372 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:50569421-50569504 | Rare:18 | ||||
| chr3:50611737-50611883 | Rare:34 | ||||
| chr3:51385012-51385345 | Common:2; Rare:102 | ||||
| chr3:52239079-52239255 | Common:2; Rare:64 | ||||
| chr3:52278620-52278791 | Rare:59 | ||||
| chr3:52455305-52455657 | Common:2; Rare:101 | ||||
| chr3:52495282-52495389 | Common:1; Rare:28 | ||||
| chr3:52536360-52536745 | Common:2; Rare:124 | ||||
| chr3:52685544-52685809 | Common:2; Rare:69 | ||||
| chr3:52685937-52686234 | Common:2; Rare:110 | ||||
| chr3:52705565-52706247 | Common:4; Rare:223 |