| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12664052-12664310 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:13420226-13420446 | Common:1; Rare:62 | ||||
| chr3:14124697-14125093 | Common:4; Rare:118; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178573-14178863 | Common:2; Rare:150; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:14402415-14402638 | Common:1; Rare:61 | ||||
| chr3:14947412-14947524 | Common:2; Rare:57 | ||||
| chr3:15427503-15427641 | Rare:45 | ||||
| chr3:15601519-15601804 | Common:4; Rare:119; Clinvar:1 | ||||
| chr3:16264862-16265220 | Common:2; Rare:121 | ||||
| chr3:17742596-17742942 | Common:4; Rare:120 | ||||
| chr3:19946974-19947203 | Common:4; Rare:84 | ||||
| chr3:20186129-20186411 | Common:4; Rare:89 | ||||
| chr3:23805828-23806015 | Common:1; Rare:37 | ||||
| chr3:23916919-23917203 | Rare:107 | ||||
| chr3:25783390-25783640 | Common:2; Rare:78; Clinvar (benign):3 |