| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5260696-5261025 | Common:3; Rare:108; Clinvar (benign):4 | ||||
| chr6:5261275-5261559 | Common:9; Rare:71 | ||||
| chr6:7313042-7313333 | Common:5; Rare:113 | ||||
| chr6:7389734-7390059 | Common:1; Rare:94 | ||||
| chr6:7541390-7541548 | Rare:58 | ||||
| chr6:7910610-7910923 | Common:4; Rare:125 | ||||
| chr6:8064307-8064601 | Common:4; Rare:94 | ||||
| chr6:8102456-8102741 | Common:1; Rare:99 | ||||
| chr6:8435361-8435659 | Common:4; Rare:105 | ||||
| chr6:10412165-10412334 | Rare:60 | ||||
| chr6:10694580-10694994 | Common:5; Rare:120 | ||||
| chr6:10722783-10723237 | Common:6; Rare:155 | ||||
| chr6:10747621-10747864 | Common:2; Rare:97 | ||||
| chr6:11094081-11094260 | Rare:50 | ||||
| chr6:13328515-13328621 | Common:2; Rare:36 |