| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201642633-201642778 | Rare:127 | ||||
| chr2:201780783-201781235 | Common:5; Rare:162; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:202238478-202238656 | Rare:61; Clinvar:1 | ||||
| chr2:202265655-202265938 | Common:1; Rare:169 | ||||
| chr2:202376066-202376620 | Common:2; Rare:236; Clinvar:5; Clinvar (benign):6 | ||||
| chr2:202376837-202377237 | Common:2; Rare:143; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:202634665-202635067 | Common:12; Rare:224 | ||||
| chr2:202911562-202912293 | Common:5; Rare:288 | ||||
| chr2:203014672-203014957 | Common:2; Rare:164 | ||||
| chr2:203238890-203239060 | Common:2; Rare:129 | ||||
| chr2:203239180-203239364 | Rare:109 | ||||
| chr2:203328047-203328437 | Common:4; Rare:250 | ||||
| chr2:203535122-203535546 | Common:5; Rare:246 | ||||
| chr2:205682351-205682510 | Rare:28 | ||||
| chr2:206085742-206086044 | Common:3; Rare:119 |