| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:4021213-4021415 | Rare:90 | ||||
| chr6:5003611-5003823 | Common:6; Rare:62 | ||||
| chr6:5260694-5261015 | Common:3; Rare:106; Clinvar (benign):4 | ||||
| chr6:7313139-7313380 | Common:4; Rare:83 | ||||
| chr6:7389740-7389868 | Common:1; Rare:38 | ||||
| chr6:7541399-7541676 | Rare:87; Clinvar (benign):1 | ||||
| chr6:8102524-8102712 | Common:1; Rare:63 | ||||
| chr6:8435491-8435654 | Common:3; Rare:65 | ||||
| chr6:10521213-10521518 | Common:1; Rare:75 | ||||
| chr6:10528408-10528536 | Rare:24 | ||||
| chr6:10694595-10694984 | Common:5; Rare:104 | ||||
| chr6:10722848-10723224 | Common:6; Rare:125 | ||||
| chr6:10747582-10747869 | Common:3; Rare:110 | ||||
| chr6:11232652-11232810 | Rare:32 | ||||
| chr6:12289867-12290082 | Common:1; Rare:26 |