| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4229371-4229535 | Common:1; Rare:51 | ||||
| chr19:4246976-4247123 | Common:1; Rare:56 | ||||
| chr19:4471981-4472333 | Common:6; Rare:135 | ||||
| chr19:4639268-4639560 | Common:1; Rare:99 | ||||
| chr19:4713656-4713923 | Common:3; Rare:85 | ||||
| chr19:4723741-4724069 | Common:7; Rare:126 | ||||
| chr19:4831684-4831793 | Common:1; Rare:26 | ||||
| chr19:4867621-4867922 | Common:4; Rare:90 | ||||
| chr19:4909876-4910237 | Common:2; Rare:96 | ||||
| chr19:5622725-5623195 | Common:5; Rare:186 | ||||
| chr19:5680473-5681172 | Rare:207 | ||||
| chr19:5903713-5903890 | Common:1; Rare:86; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:5978078-5978413 | Common:3; Rare:128 | ||||
| chr19:6110476-6110831 | Common:2; Rare:107 | ||||
| chr19:6361733-6361874 | Rare:65; Clinvar:1 |