| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88055739-88055911 | Rare:67 | ||||
| chr2:96265978-96266281 | Common:2; Rare:90 | ||||
| chr2:96305488-96305657 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:96335697-96335779 | Common:1; Rare:27 | ||||
| chr2:98608461-98608636 | Common:1; Rare:75 | ||||
| chr2:99180986-99181213 | Common:2; Rare:68 | ||||
| chr2:101002129-101002325 | Rare:75 | ||||
| chr2:105337454-105337580 | Common:1; Rare:59 | ||||
| chr2:106194286-106194573 | Common:4; Rare:108 | ||||
| chr2:108534203-108534477 | Common:7; Rare:113 | ||||
| chr2:108719383-108719482 | Common:1; Rare:38 | ||||
| chr2:112584388-112584633 | Common:1; Rare:66 | ||||
| chr2:113627068-113627235 | Rare:48 | ||||
| chr2:119366804-119367059 | Common:1; Rare:74 | ||||
| chr2:130181561-130181622 | Common:1; Rare:23 |