| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41921069-41921237 | Common:1; Rare:47 | ||||
| chr6:41921353-41921732 | Common:3; Rare:133 | ||||
| chr6:41941468-41941669 | Rare:52 | ||||
| chr6:41941711-41942017 | Common:1; Rare:92 | ||||
| chr6:42142434-42142711 | Common:2; Rare:72 | ||||
| chr6:42451209-42451358 | Rare:44 | ||||
| chr6:42451502-42451937 | Common:2; Rare:96 | ||||
| chr6:42452024-42452329 | Common:2; Rare:53 | ||||
| chr6:42746080-42746354 | Rare:70 | ||||
| chr6:42879577-42879964 | Rare:121 | ||||
| chr6:42929098-42929561 | Common:4; Rare:130 | ||||
| chr6:42979165-42979317 | Common:3; Rare:47; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:42984281-42984619 | Rare:84 | ||||
| chr6:43006976-43007246 | Rare:66 | ||||
| chr6:43008435-43008731 | Common:1; Rare:67 |