| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4303222-4303658 | Common:4; Rare:166 | ||||
| chr3:4467201-4467313 | Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493151-4493548 | Common:1; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:4979125-4979631 | Common:2; Rare:113 | ||||
| chr3:4980368-4980517 | Rare:39 | ||||
| chr3:5122441-5122492 | Common:1; Rare:17 | ||||
| chr3:5174271-5174411 | Rare:28 | ||||
| chr3:5187251-5187718 | Common:5; Rare:172 | ||||
| chr3:8501523-8501590 | Rare:14 | ||||
| chr3:8501635-8501969 | Common:2; Rare:119 | ||||
| chr3:9249617-9249750 | Common:1; Rare:35 | ||||
| chr3:9362934-9363164 | Common:2; Rare:74 | ||||
| chr3:9397019-9397155 | Common:1; Rare:39 | ||||
| chr3:9397427-9397918 | Common:1; Rare:156 | ||||
| chr3:9749814-9750329 | Common:2; Rare:163 |