| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219497821-219498498 | Common:9; Rare:265 | ||||
| chr2:219498413-219498985 | Common:9; Rare:300 | ||||
| chr2:219542981-219543289 | Common:5; Rare:117 | ||||
| chr2:219543525-219544076 | Common:9; Rare:388 | ||||
| chr2:219552277-219552590 | Common:4; Rare:178; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:219570583-219570750 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:219571351-219571734 | Common:3; Rare:185; Clinvar:10 | ||||
| chr2:219571854-219572362 | Common:37; Rare:293 | ||||
| chr2:219597576-219597926 | Common:4; Rare:330 | ||||
| chr2:219598019-219598287 | Common:3; Rare:222 | ||||
| chr2:219627500-219627821 | Common:3; Rare:126 | ||||
| chr2:221572172-221572574 | Common:14; Rare:319 | ||||
| chr2:222424000-222424660 | Common:1; Rare:287 | ||||
| chr2:222655867-222656530 | Common:7; Rare:369 | ||||
| chr2:222860760-222861151 | Common:6; Rare:366 |