| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:180810102-180810229 | Common:1; Rare:28 | ||||
| chr5:180861214-180861598 | Common:4; Rare:126 | ||||
| chr5:181223118-181223313 | Rare:66 | ||||
| chr5:181223620-181223768 | Common:3; Rare:33 | ||||
| chr5:181261074-181261223 | Rare:45 | ||||
| chr6:693064-693199 | Rare:42 | ||||
| chr6:2245438-2245833 | Common:1; Rare:134 | ||||
| chr6:2999607-3000032 | Common:10; Rare:92 | ||||
| chr6:3118611-3118752 | Common:2; Rare:46 | ||||
| chr6:3157530-3157633 | Common:6; Rare:43 | ||||
| chr6:3231730-3231802 | Rare:10 | ||||
| chr6:4021216-4021423 | Rare:96 | ||||
| chr6:5003662-5003843 | Common:5; Rare:56 | ||||
| chr6:5260679-5260996 | Common:3; Rare:106; Clinvar (benign):4 | ||||
| chr6:7389740-7389881 | Common:1; Rare:41 |