| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108449016-108449257 | Common:1; Rare:88 | ||||
| chr2:108534151-108534497 | Common:7; Rare:139 | ||||
| chr2:108719311-108719566 | Common:3; Rare:109; Clinvar (benign):1 | ||||
| chr2:111884100-111884244 | Rare:43 | ||||
| chr2:112255019-112255150 | Common:1; Rare:58 | ||||
| chr2:112542115-112542492 | Common:1; Rare:117 | ||||
| chr2:112584280-112584633 | Common:2; Rare:97 | ||||
| chr2:112645633-112645939 | Common:2; Rare:102 | ||||
| chr2:112764591-112764836 | Common:2; Rare:77; Clinvar (pathogenic):1 | ||||
| chr2:113627065-113627272 | Common:1; Rare:62 | ||||
| chr2:113889710-113890165 | Common:8; Rare:151 | ||||
| chr2:118088223-118088516 | Common:2; Rare:82 | ||||
| chr2:119366795-119367070 | Common:1; Rare:83 | ||||
| chr2:120252616-120252961 | Common:3; Rare:114 | ||||
| chr2:121530619-121530885 | Common:5; Rare:113 |