| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:21298037-21298160 | Common:2; Rare:32 | ||||
| chr13:29140318-29140541 | Rare:36 | ||||
| chr13:51826740-51826967 | Common:2; Rare:44 | ||||
| chr13:52617322-52617537 | Rare:52 | ||||
| chr13:97990215-97990480 | Common:1; Rare:60 | ||||
| chr13:101868745-101868958 | Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:102394511-102394660 | Common:1; Rare:57 | ||||
| chr13:110205351-110205530 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:20456828-20457139 | Common:2; Rare:122; Clinvar:1 | ||||
| chr14:22770572-22770902 | Common:2; Rare:76 | ||||
| chr14:23387527-23387924 | Common:2; Rare:147; Clinvar:11; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr14:23389391-23389620 | Rare:82; Clinvar:10; Clinvar (benign):9 | ||||
| chr14:23392565-23392952 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 | ||||
| chr14:23393489-23393909 | Common:3; Rare:102; Clinvar:8; Clinvar (benign):8 | ||||
| chr14:23402695-23402931 | Common:2; Rare:56; Clinvar:6; Clinvar (benign):3 |