| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124538981-124539287 | Common:2; Rare:157; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124673330-124673678 | Common:2; Rare:66 | ||||
| chr8:125091691-125091877 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:126558389-126558628 | Common:1; Rare:86 | ||||
| chr8:127735864-127736076 | Rare:45 | ||||
| chr8:133570353-133570572 | Rare:50 | ||||
| chr8:133571793-133572270 | Common:1; Rare:123 | ||||
| chr8:134713017-134713161 | Common:1; Rare:47 | ||||
| chr8:140511257-140511547 | Common:2; Rare:115 | ||||
| chr8:141001149-141001431 | Common:2; Rare:94 | ||||
| chr8:142403118-142403334 | Rare:66 | ||||
| chr8:142700402-142700505 | Common:3; Rare:48 | ||||
| chr8:142726998-142727258 | Common:4; Rare:99 | ||||
| chr8:143018388-143018545 | Common:1; Rare:47 | ||||
| chr8:143213009-143213280 | Common:1; Rare:73 |