| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4722711-4722913 | Common:1; Rare:48 | ||||
| chr19:4723691-4723863 | Common:1; Rare:58 | ||||
| chr19:4831641-4831770 | Common:3; Rare:38 | ||||
| chr19:4867626-4867814 | Common:3; Rare:56 | ||||
| chr19:5293213-5293396 | Common:1; Rare:84 | ||||
| chr19:5622729-5623388 | Common:6; Rare:250 | ||||
| chr19:5720135-5720347 | Rare:79 | ||||
| chr19:5978078-5978415 | Common:3; Rare:130 | ||||
| chr19:6372464-6372827 | Common:5; Rare:118 | ||||
| chr19:6393371-6393769 | Common:5; Rare:117 | ||||
| chr19:6679123-6679508 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:6684773-6685155 | Rare:100; Clinvar (benign):1 | ||||
| chr19:6693410-6693643 | Common:2; Rare:64; Clinvar (benign):1 | ||||
| chr19:6710637-6711207 | Common:3; Rare:176; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:6714144-6714455 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):2 |