| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112784461-112784615 | Rare:35 | ||||
| chr2:112836774-112836945 | Common:1; Rare:26; Clinvar:1 | ||||
| chr2:113157136-113157419 | Common:2; Rare:64 | ||||
| chr2:113173605-113173704 | Rare:17 | ||||
| chr2:113173741-113174044 | Common:3; Rare:55 | ||||
| chr2:113174131-113174239 | Common:1; Rare:15 | ||||
| chr2:113235439-113235599 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:113626760-113626811 | Common:1; Rare:8 | ||||
| chr2:113627078-113627243 | Rare:43 | ||||
| chr2:113756123-113756276 | Common:1; Rare:42 | ||||
| chr2:113756496-113757153 | Common:7; Rare:184 | ||||
| chr2:113889619-113890260 | Common:8; Rare:199 | ||||
| chr2:113890715-113891345 | Common:1; Rare:128 | ||||
| chr2:117814401-117814814 | Common:1; Rare:128 | ||||
| chr2:117814918-117815012 | Rare:23 |