| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23916887-23917177 | Rare:110 | ||||
| chr3:25428107-25428289 | Rare:34 | ||||
| chr3:28349025-28349162 | Common:2; Rare:38 | ||||
| chr3:33097104-33097279 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:37243216-37243344 | Common:1; Rare:36 | ||||
| chr3:40309531-40309816 | Common:7; Rare:99 | ||||
| chr3:42581932-42582137 | Common:3; Rare:56 | ||||
| chr3:42600383-42600703 | Common:2; Rare:127 | ||||
| chr3:44761598-44761810 | Common:3; Rare:75 | ||||
| chr3:44861796-44861918 | Common:2; Rare:56 | ||||
| chr3:44976126-44976272 | Common:2; Rare:63 | ||||
| chr3:45842094-45842295 | Common:1; Rare:53 | ||||
| chr3:47475821-47476058 | Common:3; Rare:102 | ||||
| chr3:48440056-48440291 | Common:1; Rare:81 | ||||
| chr3:48504156-48504263 | Common:1; Rare:26 |