| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:236972650-236973100 | Common:6; Rare:117 | ||||
| chr2:236986480-236986940 | Common:9; Rare:169 | ||||
| chr2:236988780-236989220 | Common:11; Rare:197 | ||||
| chr2:236997878-236998642 | Common:12; Rare:218 | ||||
| chr2:237009610-237009960 | Common:1; Rare:76 | ||||
| chr2:237025080-237025454 | Common:3; Rare:105 | ||||
| chr2:237027440-237027840 | Common:6; Rare:109 | ||||
| chr2:237041105-237041665 | Common:5; Rare:280 | ||||
| chr2:237075986-237076600 | Common:2; Rare:158 | ||||
| chr2:237315313-237315515 | Common:1; Rare:38 | ||||
| chr2:237432707-237432894 | Common:3; Rare:33 | ||||
| chr2:237471384-237471802 | Common:7; Rare:118 | ||||
| chr2:237473552-237473841 | Common:1; Rare:120 | ||||
| chr2:237473858-237474258 | Common:3; Rare:172 | ||||
| chr2:237474490-237474774 | Rare:58 |