| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:182143827-182144032 | Common:2; Rare:46 | ||||
| chr4:183659156-183659379 | Common:1; Rare:72 | ||||
| chr4:184474502-184474765 | Rare:60 | ||||
| chr4:184649408-184649786 | Common:4; Rare:126 | ||||
| chr4:185396431-185396708 | Rare:97 | ||||
| chr4:185396717-185396843 | Rare:34 | ||||
| chr4:185425951-185426252 | Common:1; Rare:79 | ||||
| chr4:186191460-186191582 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:189940593-189941007 | Common:16; Rare:142 | ||||
| chr5:218117-218364 | Common:3; Rare:102; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:443103-443206 | Common:2; Rare:43 | ||||
| chr5:892765-892999 | Common:1; Rare:90 | ||||
| chr5:1345019-1345206 | Common:1; Rare:65 | ||||
| chr5:1799781-1799949 | Common:8; Rare:84 | ||||
| chr5:1801360-1801420 | Common:1; Rare:23; Clinvar (benign):1 |