| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137219342-137219535 | Common:4; Rare:70; Clinvar (benign):2 | ||||
| chr6:137866935-137867268 | Rare:78 | ||||
| chr6:138106851-138107680 | Common:13; Rare:312 | ||||
| chr6:138404077-138404258 | Common:1; Rare:46 | ||||
| chr6:138499372-138499655 | Common:2; Rare:53 | ||||
| chr6:138545730-138545955 | Common:1; Rare:42 | ||||
| chr6:138572431-138572731 | Common:2; Rare:62 | ||||
| chr6:138692270-138692620 | Common:2; Rare:82 | ||||
| chr6:138773273-138773481 | Common:2; Rare:40 | ||||
| chr6:138773669-138773807 | Common:3; Rare:66 | ||||
| chr6:138987173-138987573 | Common:6; Rare:116 | ||||
| chr6:138988140-138988570 | Common:3; Rare:108 | ||||
| chr6:139028445-139028754 | Rare:62 | ||||
| chr6:139029088-139029193 | Common:1; Rare:28 | ||||
| chr6:139134748-139135148 | Common:2; Rare:192 |