| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5903704-5903890 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:5978059-5978415 | Common:3; Rare:138 | ||||
| chr19:6110405-6110838 | Common:2; Rare:132 | ||||
| chr19:6361722-6361801 | Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6416839-6417066 | Common:1; Rare:79 | ||||
| chr19:6468939-6469220 | Common:6; Rare:55 | ||||
| chr19:6741112-6741231 | Rare:43 | ||||
| chr19:7294436-7294554 | Common:1; Rare:35 | ||||
| chr19:7395014-7395203 | Common:6; Rare:59 | ||||
| chr19:7488993-7489103 | Rare:50 | ||||
| chr19:7535574-7535791 | Common:3; Rare:79 | ||||
| chr19:7616385-7616622 | Common:3; Rare:51 | ||||
| chr19:7629500-7629859 | Common:7; Rare:132; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636969-7637152 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr19:7903515-7903967 | Common:1; Rare:146 |