| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54114920-54115530 | Common:9; Rare:341; Clinvar (benign):7 | ||||
| chr19:54115535-54115935 | Common:16; Rare:414; Clinvar:36; Clinvar (benign):2 | ||||
| chr19:54137022-54137803 | Common:18; Rare:637 | ||||
| chr19:54159303-54160203 | Common:7; Rare:1427 | ||||
| chr19:54160508-54161079 | Common:2; Rare:249 | ||||
| chr19:54164645-54165079 | Common:5; Rare:144 | ||||
| chr19:54180617-54181401 | Common:4; Rare:351; Clinvar (pathogenic):2 | ||||
| chr19:54188240-54188610 | Common:9; Rare:458 | ||||
| chr19:54188521-54190133 | Common:38; Rare:1297 | ||||
| chr19:54190039-54190374 | Common:9; Rare:292; Clinvar:3 | ||||
| chr19:54190400-54190804 | Common:14; Rare:318; Clinvar (benign):2 | ||||
| chr19:54190716-54192322 | Common:33; Rare:1406; Clinvar:19; Clinvar (benign):18 | ||||
| chr19:54200488-54200989 | Common:30; Rare:709 | ||||
| chr19:54201000-54201198 | Common:9; Rare:227 | ||||
| chr19:54201473-54201873 | Common:4; Rare:111 |