| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:30744058-30744421 | Common:5; Rare:121 | ||||
| chr8:31033594-31033889 | Common:4; Rare:70; Clinvar:5; Clinvar (benign):4 | ||||
| chr8:33485058-33485219 | Common:2; Rare:57 | ||||
| chr8:33567120-33567315 | Common:4; Rare:56 | ||||
| chr8:37736561-37736754 | Common:3; Rare:48 | ||||
| chr8:37762478-37762687 | Common:2; Rare:75 | ||||
| chr8:38105356-38105563 | Common:2; Rare:63 | ||||
| chr8:38105783-38105966 | Rare:51 | ||||
| chr8:38176430-38176869 | Common:5; Rare:125 | ||||
| chr8:38231521-38231781 | Rare:71 | ||||
| chr8:38269125-38269238 | Rare:46 | ||||
| chr8:38466220-38466301 | Common:1; Rare:22 | ||||
| chr8:38467989-38468168 | Rare:49; Clinvar (benign):2 | ||||
| chr8:38728117-38728681 | Common:4; Rare:102 | ||||
| chr8:38786996-38787244 | Rare:93 |