| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:111884105-111884255 | Rare:45 | ||||
| chr2:112254990-112255193 | Common:2; Rare:86 | ||||
| chr2:112275408-112275617 | Common:1; Rare:63 | ||||
| chr2:112275930-112276005 | Rare:23 | ||||
| chr2:112542109-112542502 | Common:2; Rare:122 | ||||
| chr2:112584307-112584633 | Common:2; Rare:88 | ||||
| chr2:112645709-112645946 | Common:1; Rare:87 | ||||
| chr2:112646105-112646436 | Common:2; Rare:105 | ||||
| chr2:112764561-112764767 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
| chr2:113437634-113437961 | Common:4; Rare:130 | ||||
| chr2:113627023-113627334 | Common:4; Rare:90 | ||||
| chr2:113756590-113756791 | Common:3; Rare:76 | ||||
| chr2:113889747-113890302 | Common:9; Rare:173 | ||||
| chr2:113890925-113891281 | Rare:69 | ||||
| chr2:117814643-117814795 | Rare:61 |