| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:2127530-2127816 | Common:13; Rare:68 | ||||
| chr8:4994646-4994870 | Common:1; Rare:83 | ||||
| chr8:6406518-6406670 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708165-6708373 | Common:3; Rare:85 | ||||
| chr8:10839819-10839952 | Rare:55 | ||||
| chr8:11802391-11802809 | Common:8; Rare:244 | ||||
| chr8:13566760-13566900 | Common:6; Rare:53 | ||||
| chr8:15540154-15540368 | Common:5; Rare:74; Clinvar:9; Clinvar (benign):1 | ||||
| chr8:17246778-17247048 | Common:2; Rare:116 | ||||
| chr8:17413288-17413508 | Common:3; Rare:118 | ||||
| chr8:18084820-18084859 | Common:1; Rare:13; Clinvar (benign):1 | ||||
| chr8:18084925-18085030 | Rare:23 | ||||
| chr8:19817304-19817492 | Common:3; Rare:69 | ||||
| chr8:20197273-20197436 | Rare:78 | ||||
| chr8:21919419-21919763 | Common:2; Rare:133 |