| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7641936-7641951 | Rare:3 | ||||
| chr19:7642029-7642332 | Common:2; Rare:105; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:7676966-7677132 | Rare:39 | ||||
| chr19:7678716-7678951 | Common:3; Rare:69 | ||||
| chr19:7903546-7903923 | Rare:120 | ||||
| chr19:7920235-7920369 | Rare:61 | ||||
| chr19:7943630-7943990 | Rare:101 | ||||
| chr19:8005498-8005825 | Common:1; Rare:115 | ||||
| chr19:8308291-8308638 | Common:2; Rare:112 | ||||
| chr19:8321308-8321703 | Common:2; Rare:159 | ||||
| chr19:8363981-8364162 | Common:1; Rare:45 | ||||
| chr19:8390036-8390453 | Common:2; Rare:117 | ||||
| chr19:8444812-8445109 | Common:2; Rare:133; Clinvar (benign):1 | ||||
| chr19:8514121-8514232 | Common:2; Rare:34 | ||||
| chr19:9140319-9140451 | Common:1; Rare:40 |