| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183659044-183659343 | Common:1; Rare:85 | ||||
| chr4:184649413-184649797 | Common:4; Rare:124 | ||||
| chr4:184734024-184734439 | Common:10; Rare:166 | ||||
| chr4:185425877-185426029 | Common:2; Rare:53 | ||||
| chr4:185535413-185535764 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:186723763-186723965 | Common:6; Rare:82 | ||||
| chr4:189940613-189940991 | Common:11; Rare:134 | ||||
| chr5:218125-218388 | Common:3; Rare:112; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:443108-443246 | Common:5; Rare:57 | ||||
| chr5:612183-612351 | Rare:66 | ||||
| chr5:892726-892958 | Common:3; Rare:87 | ||||
| chr5:1799784-1799988 | Common:7; Rare:96 | ||||
| chr5:1801300-1801465 | Common:4; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378491-6378678 | Rare:78 | ||||
| chr5:6633284-6633429 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):1 |