| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46699350-46699510 | Common:2; Rare:46 | ||||
| chr2:46699530-46699980 | Common:4; Rare:173 | ||||
| chr2:46913325-46913725 | Common:2; Rare:82 | ||||
| chr2:46913626-46913831 | Common:4; Rare:66 | ||||
| chr2:46913910-46915032 | Common:8; Rare:470 | ||||
| chr2:46915200-46915600 | Common:3; Rare:118 | ||||
| chr2:46915641-46916250 | Common:25; Rare:884; Clinvar:16; Clinvar (benign):7 | ||||
| chr2:46916232-46916632 | Common:2; Rare:88 | ||||
| chr2:46940511-46940911 | Common:6; Rare:115 | ||||
| chr2:46940920-46941364 | Common:11; Rare:499 | ||||
| chr2:46941317-46941600 | Common:5; Rare:119; Clinvar (benign):1 | ||||
| chr2:46941529-46942245 | Common:19; Rare:461; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:47174613-47175013 | Common:2; Rare:103 | ||||
| chr2:47175600-47176080 | Common:15; Rare:415 | ||||
| chr2:47176364-47177054 | Common:37; Rare:1473; Clinvar (benign):23 |