| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118014017-118014229 | Common:2; Rare:114 | ||||
| chr2:118088145-118088523 | Common:2; Rare:102 | ||||
| chr2:119223706-119223871 | Rare:51 | ||||
| chr2:119366742-119367065 | Common:1; Rare:95 | ||||
| chr2:119678972-119679225 | Common:5; Rare:69 | ||||
| chr2:119759782-119759860 | Common:1; Rare:24 | ||||
| chr2:120252606-120252967 | Common:3; Rare:118 | ||||
| chr2:121530579-121530884 | Common:7; Rare:127 | ||||
| chr2:121649435-121649715 | Common:2; Rare:82 | ||||
| chr2:121736723-121737118 | Common:5; Rare:162 | ||||
| chr2:121755421-121755759 | Common:4; Rare:113 | ||||
| chr2:127294077-127294250 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127526425-127526550 | Common:2; Rare:46 | ||||
| chr2:127526792-127526870 | Rare:17 | ||||
| chr2:127811121-127811254 | Rare:42 |