| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108719351-108719566 | Common:3; Rare:93; Clinvar (benign):1 | ||||
| chr2:109613875-109614008 | Common:2; Rare:46 | ||||
| chr2:110115808-110115944 | Common:2; Rare:32 | ||||
| chr2:112275399-112275594 | Common:1; Rare:61 | ||||
| chr2:112584362-112584637 | Common:1; Rare:73 | ||||
| chr2:112645731-112645944 | Rare:77 | ||||
| chr2:113627047-113627289 | Common:2; Rare:74 | ||||
| chr2:113756556-113756735 | Common:1; Rare:56 | ||||
| chr2:113889682-113890161 | Common:8; Rare:158 | ||||
| chr2:118014037-118014237 | Common:2; Rare:110 | ||||
| chr2:118088171-118088521 | Common:2; Rare:93 | ||||
| chr2:119366784-119367068 | Common:1; Rare:87 | ||||
| chr2:119431731-119431875 | Common:3; Rare:37 | ||||
| chr2:119678960-119679222 | Common:5; Rare:71 | ||||
| chr2:121285200-121285323 | Rare:38 |