| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:103562732-103562885 | Common:7; Rare:63 | ||||
| chr5:108380806-108381035 | Common:2; Rare:80 | ||||
| chr5:108382056-108382186 | Common:1; Rare:45 | ||||
| chr5:108748326-108748463 | Common:4; Rare:25 | ||||
| chr5:108748679-108748993 | Common:2; Rare:109 | ||||
| chr5:109408925-109409120 | Common:4; Rare:51 | ||||
| chr5:109409849-109410227 | Common:4; Rare:147 | ||||
| chr5:110738906-110739124 | Common:2; Rare:88 | ||||
| chr5:111092209-111092442 | Common:2; Rare:119; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:111512395-111512875 | Common:4; Rare:150 | ||||
| chr5:111756244-111756353 | Common:2; Rare:17 | ||||
| chr5:111757108-111757508 | Common:6; Rare:106 | ||||
| chr5:111757526-111757815 | Common:1; Rare:112 | ||||
| chr5:111757946-111758144 | Common:2; Rare:68 | ||||
| chr5:112419255-112419580 | Common:3; Rare:112 |