| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:103562760-103562867 | Common:7; Rare:53 | ||||
| chr5:108380815-108381078 | Common:3; Rare:96 | ||||
| chr5:108382063-108382194 | Common:3; Rare:44 | ||||
| chr5:108748688-108748993 | Common:2; Rare:103 | ||||
| chr5:109409841-109410322 | Common:4; Rare:182 | ||||
| chr5:110738888-110739128 | Common:2; Rare:95 | ||||
| chr5:111092209-111092459 | Common:2; Rare:126; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:111224045-111224509 | Common:2; Rare:170 | ||||
| chr5:111512445-111512740 | Common:3; Rare:107 | ||||
| chr5:111756244-111756353 | Common:2; Rare:17 | ||||
| chr5:111757123-111757272 | Common:5; Rare:29 | ||||
| chr5:111757365-111757815 | Common:1; Rare:161 | ||||
| chr5:111757946-111758100 | Common:2; Rare:56 | ||||
| chr5:112419248-112419293 | Common:1; Rare:20 | ||||
| chr5:112707363-112707668 | Common:8; Rare:133; Clinvar:72; Clinvar (benign):14; Clinvar (pathogenic):1 |