| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136289239-136289472 | Rare:96 | ||||
| chr6:136289767-136290063 | Common:2; Rare:132 | ||||
| chr6:136526131-136526291 | Common:3; Rare:34 | ||||
| chr6:136526544-136526661 | Common:1; Rare:24 | ||||
| chr6:136550414-136550676 | Common:2; Rare:75 | ||||
| chr6:136792509-136792684 | Common:2; Rare:54 | ||||
| chr6:137219310-137219535 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138403996-138404601 | Common:8; Rare:180 | ||||
| chr6:138773324-138773540 | Common:3; Rare:92 | ||||
| chr6:138773646-138773827 | Common:3; Rare:86 | ||||
| chr6:139028628-139028906 | Common:1; Rare:57 | ||||
| chr6:139029025-139029146 | Common:5; Rare:28 | ||||
| chr6:139374499-139374788 | Common:1; Rare:116 | ||||
| chr6:142147086-142147336 | Common:3; Rare:108 | ||||
| chr6:143060724-143060928 | Common:7; Rare:72 |