| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158671276-158671461 | Common:2; Rare:29 | ||||
| chr4:158671817-158672435 | Common:5; Rare:165; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723026-158723191 | Rare:50 | ||||
| chr4:158723286-158723578 | Common:2; Rare:117 | ||||
| chr4:158768744-158769080 | Common:1; Rare:105 | ||||
| chr4:159103612-159103898 | Common:2; Rare:87 | ||||
| chr4:159103967-159104156 | Common:1; Rare:70 | ||||
| chr4:163166201-163166258 | Rare:14 | ||||
| chr4:163166420-163166475 | Common:1; Rare:24 | ||||
| chr4:163166753-163167024 | Common:3; Rare:94 | ||||
| chr4:163494247-163494790 | Common:7; Rare:191 | ||||
| chr4:163494923-163495258 | Common:3; Rare:82 | ||||
| chr4:164876470-164876700 | Common:2; Rare:31 | ||||
| chr4:164876993-164877312 | Common:3; Rare:44 | ||||
| chr4:164956788-164957090 | Common:6; Rare:91 |