| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27100162-27100290 | Common:1; Rare:68; Clinvar:6; Clinvar (benign):2 | ||||
| chr10:27100406-27100691 | Common:4; Rare:74; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27153730-27153983 | Common:2; Rare:57 | ||||
| chr10:27153997-27154163 | Common:3; Rare:42 | ||||
| chr10:27154280-27154521 | Rare:68 | ||||
| chr10:27154834-27154982 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:27155088-27155470 | Common:7; Rare:142; Clinvar:5; Clinvar (benign):8 | ||||
| chr10:27240292-27240419 | Rare:35 | ||||
| chr10:27240462-27240721 | Common:2; Rare:76 | ||||
| chr10:27240738-27241000 | Common:2; Rare:60 | ||||
| chr10:27241747-27241981 | Common:1; Rare:54 | ||||
| chr10:27241985-27242349 | Common:2; Rare:136 | ||||
| chr10:27503961-27504367 | Common:1; Rare:161; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:27504500-27504698 | Rare:68 | ||||
| chr10:28532072-28532182 | Common:2; Rare:27 |