| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197434970-197435198 | Rare:76 | ||||
| chr2:197499807-197500720 | Common:1; Rare:322; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515774-197516098 | Common:2; Rare:111 | ||||
| chr2:197675393-197675780 | Common:10; Rare:80 | ||||
| chr2:197675790-197675818 | Rare:5 | ||||
| chr2:197705212-197705396 | Common:2; Rare:71 | ||||
| chr2:199911073-199911361 | Rare:80 | ||||
| chr2:200306468-200306917 | Common:3; Rare:136 | ||||
| chr2:200509913-200510216 | Common:1; Rare:106 | ||||
| chr2:200811431-200811589 | Common:1; Rare:57 | ||||
| chr2:200811760-200811964 | Rare:81 | ||||
| chr2:200864228-200864264 | Rare:13 | ||||
| chr2:200864566-200864788 | Common:1; Rare:82 | ||||
| chr2:200888974-200889451 | Common:3; Rare:150 | ||||
| chr2:200963575-200963865 | Common:1; Rare:80 |