| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:134318056-134318128 | Common:1; Rare:15 | ||||
| chr6:135054765-135054980 | Common:6; Rare:65 | ||||
| chr6:135497580-135497809 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:135851469-135851786 | Rare:51 | ||||
| chr6:136038157-136038211 | Common:1; Rare:14 | ||||
| chr6:136289746-136290068 | Common:2; Rare:144 | ||||
| chr6:136822544-136822668 | Common:4; Rare:64; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:138773646-138773878 | Common:3; Rare:102 | ||||
| chr6:139028623-139028909 | Common:1; Rare:61 | ||||
| chr6:139374399-139374663 | Common:3; Rare:117 | ||||
| chr6:142147013-142147389 | Common:3; Rare:144 | ||||
| chr6:142301842-142302135 | Common:6; Rare:84 | ||||
| chr6:142944474-142944724 | Rare:58 | ||||
| chr6:143060724-143061051 | Common:8; Rare:113 | ||||
| chr6:143450570-143450961 | Common:1; Rare:143; Clinvar:4; Clinvar (benign):1 |