| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:181040121-181040312 | Rare:36 | ||||
| chr5:181223083-181223319 | Rare:82 | ||||
| chr5:181243685-181243875 | Common:2; Rare:59 | ||||
| chr5:181261065-181261290 | Rare:76 | ||||
| chr6:291990-292320 | Common:1; Rare:56 | ||||
| chr6:2841834-2841970 | Common:1; Rare:23 | ||||
| chr6:2971515-2971864 | Common:1; Rare:90 | ||||
| chr6:2988608-2988663 | Common:1; Rare:12 | ||||
| chr6:2999644-2999999 | Common:10; Rare:74 | ||||
| chr6:3063793-3063975 | Common:1; Rare:68 | ||||
| chr6:4021213-4021423 | Rare:96 | ||||
| chr6:5004006-5004112 | Common:1; Rare:52 | ||||
| chr6:5260685-5261011 | Common:3; Rare:108; Clinvar (benign):4 | ||||
| chr6:7313098-7313380 | Common:5; Rare:105 | ||||
| chr6:7541334-7542084 | Common:6; Rare:247; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 |