| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136289213-136289477 | Rare:102 | ||||
| chr6:136289767-136290063 | Common:2; Rare:132 | ||||
| chr6:136550361-136550687 | Common:2; Rare:97 | ||||
| chr6:137219334-137219466 | Common:2; Rare:49; Clinvar (benign):2 | ||||
| chr6:137866931-137867513 | Rare:127 | ||||
| chr6:137867728-137867791 | Rare:13 | ||||
| chr6:137870721-137870793 | Rare:15 | ||||
| chr6:137870804-137871150 | Common:2; Rare:63 | ||||
| chr6:138106980-138107099 | Common:2; Rare:25 | ||||
| chr6:138107249-138107450 | Rare:67 | ||||
| chr6:138572379-138572726 | Common:3; Rare:68 | ||||
| chr6:138692042-138692215 | Common:4; Rare:50 | ||||
| chr6:138692496-138692554 | Common:1; Rare:14 | ||||
| chr6:138773311-138773616 | Common:3; Rare:117 | ||||
| chr6:138773646-138773827 | Common:3; Rare:86 |