| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143597093-143597240 | Common:1; Rare:49 | ||||
| chr8:143617458-143617759 | Common:2; Rare:113 | ||||
| chr8:143635969-143636107 | Common:2; Rare:60 | ||||
| chr8:143684275-143684489 | Common:2; Rare:58 | ||||
| chr8:143733713-143734063 | Common:1; Rare:102 | ||||
| chr8:143808860-143809202 | Common:4; Rare:140 | ||||
| chr8:143829300-143829544 | Rare:102 | ||||
| chr8:143939360-143939728 | Common:3; Rare:142; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr8:143986381-143986494 | Rare:21 | ||||
| chr8:143991063-143991318 | Rare:80 | ||||
| chr8:144060670-144060846 | Rare:53 | ||||
| chr8:144063387-144063577 | Rare:47 | ||||
| chr8:144078532-144078722 | Common:1; Rare:57 | ||||
| chr8:144082503-144082689 | Common:2; Rare:65 | ||||
| chr8:144094825-144095228 | Common:4; Rare:120; Clinvar (benign):2 |