| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1071134-1071249 | Rare:29 | ||||
| chr19:1071579-1071668 | Common:1; Rare:20 | ||||
| chr19:1095280-1095600 | Common:8; Rare:139 | ||||
| chr19:1103720-1104152 | Common:8; Rare:174 | ||||
| chr19:1104321-1104793 | Common:5; Rare:110 | ||||
| chr19:1132203-1132336 | Rare:56 | ||||
| chr19:1173291-1173863 | Common:3; Rare:138 | ||||
| chr19:1174162-1174379 | Common:1; Rare:101 | ||||
| chr19:1205385-1205888 | Common:2; Rare:161; Clinvar:1 | ||||
| chr19:1207004-1207213 | Common:1; Rare:57; Clinvar:13; Clinvar (benign):23; Clinvar (pathogenic):2 | ||||
| chr19:1237834-1238171 | Common:2; Rare:102 | ||||
| chr19:1241585-1241868 | Rare:90 | ||||
| chr19:1248435-1248750 | Common:1; Rare:113 | ||||
| chr19:1248886-1249195 | Common:2; Rare:85 | ||||
| chr19:1249305-1249936 | Common:3; Rare:244 |