| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:157731390-157731462 | Common:2; Rare:33 | ||||
| chr5:159263201-159263342 | Common:1; Rare:47 | ||||
| chr5:160213601-160213791 | Common:1; Rare:50 | ||||
| chr5:160370633-160370954 | Rare:68 | ||||
| chr5:160400010-160400168 | Rare:54 | ||||
| chr5:160419022-160419171 | Common:2; Rare:49 | ||||
| chr5:161546746-161547073 | Common:1; Rare:55; Clinvar (benign):2 | ||||
| chr5:161547492-161547587 | Rare:21 | ||||
| chr5:161547613-161547881 | Rare:70 | ||||
| chr5:161548162-161548253 | Rare:17 | ||||
| chr5:161548359-161548429 | Rare:11 | ||||
| chr5:161847116-161847194 | Rare:14 | ||||
| chr5:161850566-161850835 | Rare:64; Clinvar (benign):5 | ||||
| chr5:162067380-162068068 | Common:2; Rare:175; Clinvar:8; Clinvar (benign):4 | ||||
| chr5:163437292-163437652 | Rare:108 |