| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112584343-112584645 | Common:1; Rare:85 | ||||
| chr2:112584782-112584854 | Rare:18 | ||||
| chr2:112645353-112645385 | Rare:12 | ||||
| chr2:112645557-112645957 | Common:2; Rare:136 | ||||
| chr2:112764588-112764815 | Common:2; Rare:74; Clinvar (pathogenic):1 | ||||
| chr2:113627079-113627303 | Common:3; Rare:63 | ||||
| chr2:113756556-113756771 | Common:3; Rare:73 | ||||
| chr2:113889709-113890320 | Common:9; Rare:192 | ||||
| chr2:113891012-113891114 | Rare:26 | ||||
| chr2:115161310-115161667 | Common:7; Rare:127 | ||||
| chr2:115162028-115162241 | Common:2; Rare:84 | ||||
| chr2:118013816-118013914 | Common:1; Rare:34 | ||||
| chr2:118013955-118014224 | Common:3; Rare:136 | ||||
| chr2:118088352-118088633 | Common:1; Rare:73 | ||||
| chr2:118088905-118088955 | Rare:7 |