| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15601460-15601807 | Common:4; Rare:143; Clinvar:2 | ||||
| chr3:15601859-15602010 | Common:1; Rare:76; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:15676983-15677182 | Common:1; Rare:47 | ||||
| chr3:15859772-15860027 | Common:1; Rare:87 | ||||
| chr3:16264818-16265267 | Common:3; Rare:157 | ||||
| chr3:16884718-16884770 | Rare:11 | ||||
| chr3:16884861-16885157 | Common:5; Rare:77 | ||||
| chr3:19946974-19947457 | Common:7; Rare:179 | ||||
| chr3:21751074-21751405 | Common:4; Rare:102 | ||||
| chr3:23202925-23203220 | Common:1; Rare:104 | ||||
| chr3:23916855-23917181 | Rare:123 | ||||
| chr3:24494300-24494471 | Common:2; Rare:37 | ||||
| chr3:24495153-24495512 | Common:5; Rare:98 | ||||
| chr3:25428107-25428296 | Rare:36 | ||||
| chr3:25790008-25790130 | Common:4; Rare:48 |