| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:55141231-55142301 | Common:19; Rare:322; Clinvar:2; Clinvar (benign):6 | ||||
| chr19:55145997-55146710 | Common:9; Rare:615; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:55146681-55147200 | Common:20; Rare:696; Clinvar:6; Clinvar (benign):25; Clinvar (pathogenic):2 | ||||
| chr19:55147270-55147670 | Common:28; Rare:102 | ||||
| chr19:55156326-55156726 | Common:7; Rare:254; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr19:55156700-55157580 | Common:26; Rare:397; Clinvar:10; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr19:55157627-55158027 | Common:3; Rare:209; Clinvar:6; Clinvar (benign):4 | ||||
| chr19:55159812-55160694 | Common:14; Rare:557; Clinvar:15; Clinvar (benign):10 | ||||
| chr19:55160638-55160987 | Common:8; Rare:348; Clinvar:12; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr19:55166293-55167242 | Common:40; Rare:1065; Clinvar:36; Clinvar (benign):27 | ||||
| chr19:55173455-55174450 | Common:45; Rare:760 | ||||
| chr19:55174642-55175341 | Common:47; Rare:634 | ||||
| chr19:55176096-55176931 | Common:18; Rare:254 | ||||
| chr19:55207076-55207482 | Common:10; Rare:599 | ||||
| chr19:55209366-55209887 | Common:9; Rare:209 |