| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:159839747-159840177 | Common:4; Rare:87 | ||||
| chr3:160399146-160399523 | Rare:112; Clinvar:7 | ||||
| chr3:160449737-160450075 | Common:2; Rare:114 | ||||
| chr3:160565535-160565835 | Common:2; Rare:107 | ||||
| chr3:160755452-160755666 | Common:1; Rare:80 | ||||
| chr3:160755922-160756292 | Common:1; Rare:92 | ||||
| chr3:161105221-161105362 | Common:1; Rare:51 | ||||
| chr3:161221196-161221366 | Common:2; Rare:56 | ||||
| chr3:161371473-161371716 | Common:3; Rare:41 | ||||
| chr3:161371922-161372167 | Rare:55 | ||||
| chr3:165195727-165195844 | Rare:32 | ||||
| chr3:165196130-165196225 | Rare:23 | ||||
| chr3:165196366-165196470 | Common:1; Rare:30 | ||||
| chr3:165196662-165197022 | Common:5; Rare:119 | ||||
| chr3:167734823-167735331 | Common:5; Rare:162; Clinvar:1; Clinvar (benign):1 |