| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41363726-41364411 | Common:2; Rare:209; Clinvar:6 | ||||
| chr19:41397259-41397508 | Common:4; Rare:79 | ||||
| chr19:41397527-41397896 | Common:8; Rare:127; Clinvar (benign):7 | ||||
| chr19:41439526-41439745 | Common:2; Rare:60 | ||||
| chr19:41439795-41439954 | Common:2; Rare:76 | ||||
| chr19:41549231-41549550 | Common:3; Rare:61 | ||||
| chr19:41575981-41576247 | Common:2; Rare:47 | ||||
| chr19:41859521-41860316 | Common:4; Rare:249; Clinvar:5; Clinvar (benign):4 | ||||
| chr19:41876766-41877325 | Common:1; Rare:103 | ||||
| chr19:41877552-41877808 | Rare:37 | ||||
| chr19:41882803-41882864 | Rare:13 | ||||
| chr19:41882981-41883282 | Common:1; Rare:59 | ||||
| chr19:41883998-41884551 | Rare:149 | ||||
| chr19:41958515-41958757 | Common:3; Rare:73 | ||||
| chr19:41959234-41959492 | Common:1; Rare:87 |