| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:106194243-106194543 | Common:6; Rare:127 | ||||
| chr2:108449091-108449268 | Rare:71 | ||||
| chr2:108719388-108719586 | Common:3; Rare:84; Clinvar (benign):2 | ||||
| chr2:109613885-109613998 | Common:1; Rare:41 | ||||
| chr2:111884147-111884247 | Rare:28 | ||||
| chr2:112255009-112255182 | Common:2; Rare:79 | ||||
| chr2:112275408-112275637 | Common:1; Rare:73 | ||||
| chr2:112584410-112584633 | Common:1; Rare:61 | ||||
| chr2:112645701-112645944 | Common:1; Rare:89 | ||||
| chr2:113437747-113437874 | Common:1; Rare:51 | ||||
| chr2:113627041-113627314 | Common:4; Rare:80 | ||||
| chr2:113756612-113756781 | Common:3; Rare:64 | ||||
| chr2:113889743-113890279 | Common:9; Rare:170 | ||||
| chr2:118014033-118014270 | Common:3; Rare:127 | ||||
| chr2:118088329-118088535 | Common:1; Rare:57 |