| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1169142-1169306 | Common:1; Rare:75 | ||||
| chr19:1173202-1173865 | Common:4; Rare:227 | ||||
| chr19:1174199-1174361 | Common:1; Rare:140 | ||||
| chr19:1177712-1178012 | Common:1; Rare:106 | ||||
| chr19:1237770-1238240 | Common:2; Rare:147 | ||||
| chr19:1241610-1241944 | Rare:169 | ||||
| chr19:1249555-1249920 | Common:3; Rare:280 | ||||
| chr19:1260801-1261239 | Common:6; Rare:265 | ||||
| chr19:1262120-1262548 | Common:4; Rare:136 | ||||
| chr19:1266410-1266722 | Common:5; Rare:213 | ||||
| chr19:1269513-1269913 | Rare:224 | ||||
| chr19:1275351-1275634 | Common:2; Rare:269 | ||||
| chr19:1275727-1276139 | Common:4; Rare:364 | ||||
| chr19:1354779-1355048 | Common:6; Rare:245 | ||||
| chr19:1383451-1384085 | Common:5; Rare:536; Clinvar (benign):2 |