| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:103415090-103415449 | Common:6; Rare:185 | ||||
| chr8:109334074-109334398 | Common:1; Rare:82 | ||||
| chr8:118951880-118952192 | Common:1; Rare:79; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119832830-119832897 | Common:1; Rare:22 | ||||
| chr8:120445103-120445421 | Common:1; Rare:73 | ||||
| chr8:124474549-124474777 | Rare:80 | ||||
| chr8:124539044-124539270 | Common:2; Rare:111; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091712-125091892 | Common:2; Rare:63; Clinvar (benign):3 | ||||
| chr8:143018393-143018569 | Common:2; Rare:53 | ||||
| chr8:143558267-143558407 | Common:1; Rare:58 | ||||
| chr8:144082503-144082685 | Common:2; Rare:64 | ||||
| chr8:144104240-144104519 | Common:1; Rare:92 | ||||
| chr8:144147802-144148061 | Common:2; Rare:60 | ||||
| chr8:144291378-144291647 | Common:1; Rare:88 | ||||
| chr8:144428497-144428729 | Common:3; Rare:89 |