| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10270560-10270890 | Common:1; Rare:58 | ||||
| chr19:10270910-10271169 | Common:3; Rare:335 | ||||
| chr19:10271131-10271531 | Common:1; Rare:119 | ||||
| chr19:10286435-10286837 | Common:6; Rare:80 | ||||
| chr19:10286816-10287696 | Common:27; Rare:1033; Clinvar:3 | ||||
| chr19:10289290-10289809 | Common:15; Rare:427 | ||||
| chr19:10289767-10290049 | Common:10; Rare:267 | ||||
| chr19:10290016-10290448 | Common:4; Rare:192 | ||||
| chr19:10290626-10291124 | Common:4; Rare:204 | ||||
| chr19:10291123-10291638 | Common:7; Rare:683 | ||||
| chr19:10305560-10305960 | Common:4; Rare:138 | ||||
| chr19:10315196-10315448 | Common:10; Rare:135 | ||||
| chr19:10315369-10316156 | Common:24; Rare:690; Clinvar (benign):43 | ||||
| chr19:10316215-10317087 | Common:4; Rare:196 | ||||
| chr19:10332867-10333450 | Rare:523 |