| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143939550-143939789 | Common:4; Rare:73 | ||||
| chr8:144078540-144078722 | Common:1; Rare:55 | ||||
| chr8:144082503-144082671 | Common:2; Rare:58 | ||||
| chr8:144103713-144103875 | Rare:53 | ||||
| chr8:144291376-144291637 | Common:1; Rare:85 | ||||
| chr8:144413548-144413712 | Rare:50; Clinvar:1 | ||||
| chr8:144517716-144518008 | Common:1; Rare:103; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:144792348-144792562 | Common:2; Rare:81 | ||||
| chr8:144901412-144901636 | Common:1; Rare:65 | ||||
| chr8:145052159-145052504 | Common:11; Rare:91 | ||||
| chr9:2015188-2015373 | Rare:47 | ||||
| chr9:2844034-2844343 | Common:5; Rare:115 | ||||
| chr9:4679491-4679710 | Common:1; Rare:96 | ||||
| chr9:6015610-6015721 | Rare:49 | ||||
| chr9:15307180-15307444 | Common:2; Rare:129 |