| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45885791-45886040 | Rare:101 | ||||
| chr19:45886035-45886252 | Common:1; Rare:191 | ||||
| chr19:45886330-45886750 | Common:17; Rare:145 | ||||
| chr19:45902532-45902998 | Common:11; Rare:351 | ||||
| chr19:45994980-45995573 | Common:6; Rare:524 | ||||
| chr19:46041000-46041500 | Common:4; Rare:80 | ||||
| chr19:46077390-46077680 | Common:2; Rare:58 | ||||
| chr19:46346670-46347175 | Common:9; Rare:296 | ||||
| chr19:46600566-46600669 | Rare:29 | ||||
| chr19:46600646-46601427 | Common:16; Rare:621; Clinvar (benign):4 | ||||
| chr19:46601819-46602330 | Common:2; Rare:182 | ||||
| chr19:46634154-46634533 | Common:3; Rare:70 | ||||
| chr19:46661080-46661650 | Rare:225 | ||||
| chr19:46713610-46714000 | Common:3; Rare:141 | ||||
| chr19:46714180-46714536 | Common:5; Rare:151 |