| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158818079-158818373 | Common:5; Rare:119 | ||||
| chr6:158819316-158819450 | Common:2; Rare:50 | ||||
| chr6:158999752-158999910 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159000146-159000282 | Common:1; Rare:35 | ||||
| chr6:159045004-159045336 | Rare:51 | ||||
| chr6:159693144-159693447 | Common:5; Rare:103 | ||||
| chr6:159693503-159693644 | Common:1; Rare:48 | ||||
| chr6:159726390-159726710 | Common:3; Rare:69 | ||||
| chr6:159726870-159727051 | Common:1; Rare:88 | ||||
| chr6:159727057-159727185 | Rare:42 | ||||
| chr6:159727315-159727673 | Common:5; Rare:143 | ||||
| chr6:159761773-159762077 | Common:5; Rare:141 | ||||
| chr6:159789545-159790033 | Common:5; Rare:161 | ||||
| chr6:159790244-159790637 | Common:11; Rare:150 | ||||
| chr6:160991557-160991822 | Common:3; Rare:80 |