| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:121641403-121641485 | Rare:14 | ||||
| chr8:122781589-122781934 | Common:3; Rare:66 | ||||
| chr8:123396356-123396519 | Common:1; Rare:81 | ||||
| chr8:123416342-123416624 | Rare:68 | ||||
| chr8:124474526-124474714 | Rare:73 | ||||
| chr8:124539042-124539195 | Common:2; Rare:85; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:125091731-125091938 | Common:2; Rare:71; Clinvar (benign):2 | ||||
| chr8:126558359-126558632 | Common:1; Rare:103 | ||||
| chr8:127735890-127736081 | Rare:44 | ||||
| chr8:132675534-132675647 | Rare:32 | ||||
| chr8:132775238-132775561 | Common:2; Rare:119 | ||||
| chr8:133297249-133297431 | Common:2; Rare:76; Clinvar:2 | ||||
| chr8:133571824-133572241 | Rare:104 | ||||
| chr8:134713017-134713149 | Common:1; Rare:44 | ||||
| chr8:140511246-140511494 | Common:2; Rare:100 |