| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:192194896-192195062 | Rare:32 | ||||
| chr2:195656833-195657351 | Common:2; Rare:155 | ||||
| chr2:196171336-196171411 | Rare:24 | ||||
| chr2:196278439-196278850 | Common:2; Rare:97 | ||||
| chr2:196639576-196639658 | Rare:15 | ||||
| chr2:196776493-196776822 | Rare:64 | ||||
| chr2:196799630-196799825 | Common:2; Rare:58 | ||||
| chr2:196926626-196926823 | Common:2; Rare:85 | ||||
| chr2:197434973-197435192 | Rare:75 | ||||
| chr2:197453244-197453571 | Rare:111 | ||||
| chr2:197453888-197454050 | Rare:48 | ||||
| chr2:197489972-197490108 | Rare:13 | ||||
| chr2:197499801-197500436 | Common:1; Rare:243; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500617-197500760 | Rare:38 | ||||
| chr2:197515808-197516141 | Common:2; Rare:119 |