| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185143035-185143290 | Common:4; Rare:74; Clinvar (benign):3 | ||||
| chr4:185396581-185396843 | Rare:83 | ||||
| chr4:185425870-185426267 | Common:4; Rare:121 | ||||
| chr4:186191447-186191852 | Common:7; Rare:130; Clinvar:3; Clinvar (benign):5 | ||||
| chr4:186723765-186723936 | Common:5; Rare:70 | ||||
| chr4:186726553-186726818 | Common:4; Rare:79 | ||||
| chr4:189940631-189941030 | Common:16; Rare:149 | ||||
| chr5:218124-218388 | Common:3; Rare:113; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:443090-443280 | Common:9; Rare:87 | ||||
| chr5:612189-612357 | Rare:68 | ||||
| chr5:693286-693551 | Common:6; Rare:75 | ||||
| chr5:732667-732909 | Common:3; Rare:36 | ||||
| chr5:891802-892110 | Common:2; Rare:77 | ||||
| chr5:892533-892923 | Common:5; Rare:118 | ||||
| chr5:1064215-1064314 | Rare:44 |