| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:113073695-113074013 | Common:2; Rare:62 | ||||
| chr1:113390201-113390588 | Common:1; Rare:98 | ||||
| chr1:113391587-113391808 | Common:1; Rare:38 | ||||
| chr1:113758754-113759094 | Common:1; Rare:77 | ||||
| chr1:113759312-113759571 | Common:4; Rare:66 | ||||
| chr1:113759868-113760003 | Rare:22 | ||||
| chr1:113904644-113905442 | Common:8; Rare:248; Clinvar (benign):3 | ||||
| chr1:113929488-113929875 | Common:4; Rare:101 | ||||
| chr1:114510563-114510837 | Rare:72 | ||||
| chr1:114510868-114511065 | Common:2; Rare:68 | ||||
| chr1:114511079-114511330 | Common:3; Rare:113 | ||||
| chr1:114581487-114581843 | Common:1; Rare:149 | ||||
| chr1:114670008-114670236 | Common:1; Rare:70 | ||||
| chr1:114716107-114716442 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr1:114716656-114716985 | Common:4; Rare:125; Clinvar:5; Clinvar (benign):3 |