| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:2270059-2270335 | Common:8; Rare:162 | ||||
| chr19:2270760-2271473 | Common:26; Rare:447 | ||||
| chr19:2328486-2328762 | Common:7; Rare:314 | ||||
| chr19:2427488-2427736 | Common:6; Rare:194 | ||||
| chr19:2456860-2457192 | Common:4; Rare:224; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:2475845-2476315 | Common:5; Rare:320 | ||||
| chr19:2783202-2783638 | Common:1; Rare:193 | ||||
| chr19:2785180-2785613 | Common:17; Rare:359 | ||||
| chr19:2819700-2820001 | Common:5; Rare:80 | ||||
| chr19:2841103-2841580 | Common:6; Rare:357 | ||||
| chr19:2900530-2901034 | Common:30; Rare:490 | ||||
| chr19:2944815-2945614 | Common:18; Rare:589 | ||||
| chr19:2977247-2977591 | Common:6; Rare:342 | ||||
| chr19:3028752-3029601 | Common:16; Rare:400 | ||||
| chr19:3061137-3061940 | Common:13; Rare:514 |