| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112542126-112542485 | Common:1; Rare:111 | ||||
| chr2:112584378-112584633 | Common:1; Rare:68 | ||||
| chr2:112645715-112645944 | Common:1; Rare:84 | ||||
| chr2:112764589-112764789 | Common:2; Rare:64; Clinvar (pathogenic):1 | ||||
| chr2:113627065-113627289 | Common:2; Rare:69 | ||||
| chr2:113756532-113756735 | Common:1; Rare:62 | ||||
| chr2:113889710-113890161 | Common:8; Rare:149 | ||||
| chr2:118014033-118014221 | Common:2; Rare:105 | ||||
| chr2:118088322-118088523 | Common:1; Rare:60 | ||||
| chr2:119366770-119367122 | Common:1; Rare:118 | ||||
| chr2:119679072-119679216 | Common:3; Rare:46 | ||||
| chr2:119759764-119759822 | Common:1; Rare:11 | ||||
| chr2:119760046-119760226 | Common:1; Rare:39 | ||||
| chr2:120252603-120252974 | Common:3; Rare:122 | ||||
| chr2:121285132-121285319 | Common:2; Rare:76 |