| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24076201-24076596 | Rare:107 | ||||
| chr2:24084313-24084498 | Common:6; Rare:77 | ||||
| chr2:24123272-24123506 | Common:1; Rare:62 | ||||
| chr2:24793089-24793191 | Rare:55 | ||||
| chr2:24971614-24971836 | Common:2; Rare:78 | ||||
| chr2:24971907-24972157 | Common:1; Rare:80 | ||||
| chr2:25041929-25042295 | Common:4; Rare:96 | ||||
| chr2:25673459-25673744 | Common:1; Rare:105 | ||||
| chr2:25878282-25878774 | Common:4; Rare:139 | ||||
| chr2:25982427-25982609 | Rare:50 | ||||
| chr2:26033663-26034313 | Common:5; Rare:223 | ||||
| chr2:26034320-26034735 | Common:3; Rare:101 | ||||
| chr2:26242691-26242853 | Common:4; Rare:27 | ||||
| chr2:26244573-26244990 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345752-26346253 | Common:2; Rare:159 |