| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208266111-208266308 | Common:6; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002506-210002664 | Common:4; Rare:58 | ||||
| chr2:210477568-210477685 | Rare:36 | ||||
| chr2:213284238-213284490 | Rare:82 | ||||
| chr2:214809628-214810002 | Common:3; Rare:134; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:215311910-215312139 | Common:8; Rare:94 | ||||
| chr2:215436017-215436380 | Common:2; Rare:106 | ||||
| chr2:216081771-216081906 | Common:1; Rare:45 | ||||
| chr2:216498740-216498894 | Common:6; Rare:65 | ||||
| chr2:216694438-216694854 | Rare:101 | ||||
| chr2:217978622-217978768 | Rare:40 | ||||
| chr2:217978785-217978931 | Common:1; Rare:39 | ||||
| chr2:218217088-218217226 | Rare:52 | ||||
| chr2:218270091-218270538 | Common:5; Rare:140; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218292479-218292644 | Common:1; Rare:50 |