| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54164676-54165101 | Common:4; Rare:126 | ||||
| chr19:54171943-54172680 | Common:9; Rare:216 | ||||
| chr19:54172720-54173010 | Common:1; Rare:150 | ||||
| chr19:54173089-54173432 | Common:7; Rare:147 | ||||
| chr19:54188207-54188947 | Common:9; Rare:309 | ||||
| chr19:54189193-54189713 | Common:14; Rare:413 | ||||
| chr19:54189986-54190607 | Common:11; Rare:340; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:54190811-54191050 | Rare:144 | ||||
| chr19:54191120-54191374 | Common:11; Rare:239; Clinvar:2; Clinvar (benign):6 | ||||
| chr19:54200605-54200945 | Common:14; Rare:289 | ||||
| chr19:54200930-54201494 | Common:10; Rare:339 | ||||
| chr19:54448359-54448650 | Common:2; Rare:84 | ||||
| chr19:54448843-54449306 | Common:10; Rare:298 | ||||
| chr19:54449347-54449572 | Common:16; Rare:198 | ||||
| chr19:54449673-54450971 | Common:34; Rare:564 |