| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201130674-201131314 | Common:4; Rare:96 | ||||
| chr2:201148152-201148309 | Rare:18 | ||||
| chr2:201149572-201149836 | Rare:50 | ||||
| chr2:201151221-201151433 | Rare:31 | ||||
| chr2:201151536-201151668 | Common:1; Rare:13 | ||||
| chr2:201198687-201198871 | Common:1; Rare:42 | ||||
| chr2:201276614-201276917 | Rare:71; Clinvar (pathogenic):1 | ||||
| chr2:201654907-201655186 | Rare:44 | ||||
| chr2:201679866-201679938 | Rare:9 | ||||
| chr2:202201892-202202022 | Rare:31 | ||||
| chr2:202266724-202266830 | Common:1; Rare:14 | ||||
| chr2:202280532-202280818 | Common:3; Rare:62 | ||||
| chr2:202309149-202309260 | Common:1; Rare:16 | ||||
| chr2:202375624-202375909 | Rare:72 | ||||
| chr2:202378130-202378256 | Rare:28 |