| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113198804-113199029 | Common:1; Rare:89 | ||||
| chr2:113219930-113220191 | Rare:60; Clinvar:3 | ||||
| chr2:113235353-113235758 | Common:1; Rare:157; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:113235759-113235816 | Common:2; Rare:9 | ||||
| chr2:113236910-113236934 | Common:1 | ||||
| chr2:113237653-113237907 | Common:3; Rare:47 | ||||
| chr2:113438303-113438502 | Common:1; Rare:39 | ||||
| chr2:113626628-113626811 | Common:3; Rare:30 | ||||
| chr2:113627054-113627272 | Common:1; Rare:64 | ||||
| chr2:113756138-113756211 | Common:1; Rare:20 | ||||
| chr2:113756433-113756952 | Common:7; Rare:154 | ||||
| chr2:113757150-113757330 | Rare:35 | ||||
| chr2:113889451-113889533 | Rare:23 | ||||
| chr2:113889609-113890181 | Common:8; Rare:178 | ||||
| chr2:113890495-113890813 | Common:1; Rare:83 |