| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88016527-88016819 | Common:10; Rare:133 | ||||
| chr2:91659912-91660021 | Rare:18 | ||||
| chr2:95526702-95527030 | Common:1; Rare:99 | ||||
| chr2:105361313-105361561 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:113584012-113584110 | Rare:25 | ||||
| chr2:127050449-127050656 | Common:7; Rare:57; Clinvar:1; Clinvar (benign):7 | ||||
| chr2:131682366-131682557 | Common:3; Rare:56 | ||||
| chr2:159764648-159764873 | Common:1; Rare:41 | ||||
| chr2:168644129-168644253 | Common:2; Rare:16 | ||||
| chr2:169510219-169510386 | Rare:47; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:176105235-176105496 | Common:1; Rare:45 | ||||
| chr2:176637574-176637736 | Common:2; Rare:52 | ||||
| chr2:177215572-177215894 | Common:1; Rare:59 | ||||
| chr2:178555110-178555280 | Rare:42; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:178583755-178584070 | Rare:77; Clinvar:5; Clinvar (benign):5 |