| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:111883699-111883769 | Common:1; Rare:19 | ||||
| chr2:111883902-111883971 | Rare:24 | ||||
| chr2:111884082-111884549 | Common:4; Rare:137 | ||||
| chr2:111884668-111884698 | Rare:5 | ||||
| chr2:111897809-111898040 | Common:3; Rare:47 | ||||
| chr2:111898209-111898673 | Common:2; Rare:116 | ||||
| chr2:111898759-111898939 | Common:2; Rare:53; Clinvar (benign):2 | ||||
| chr2:112055049-112055390 | Common:5; Rare:91 | ||||
| chr2:112055391-112055760 | Common:5; Rare:113 | ||||
| chr2:112138303-112138442 | Rare:37 | ||||
| chr2:112138618-112138765 | Rare:58 | ||||
| chr2:112254773-112255197 | Common:3; Rare:155 | ||||
| chr2:112275283-112275755 | Common:1; Rare:158 | ||||
| chr2:112275814-112276413 | Rare:173 | ||||
| chr2:112481908-112482237 | Common:1; Rare:115 |