| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136550355-136550717 | Common:2; Rare:111 | ||||
| chr6:137219111-137219204 | Common:1; Rare:27 | ||||
| chr6:137219284-137219511 | Common:4; Rare:79; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:137866898-137867310 | Rare:96 | ||||
| chr6:138161871-138162089 | Common:4; Rare:80 | ||||
| chr6:138404041-138404268 | Common:2; Rare:70 | ||||
| chr6:138405894-138406002 | Rare:22 | ||||
| chr6:138499364-138499634 | Common:2; Rare:49 | ||||
| chr6:138773698-138773865 | Common:3; Rare:79 | ||||
| chr6:138988268-138988377 | Rare:23 | ||||
| chr6:139028281-139028875 | Common:2; Rare:111 | ||||
| chr6:139374418-139374764 | Common:4; Rare:139 | ||||
| chr6:142147140-142147290 | Rare:56 | ||||
| chr6:142301832-142302179 | Common:6; Rare:99 | ||||
| chr6:143060683-143060926 | Common:8; Rare:88 |