| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51026349-51026621 | Common:5; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:51047824-51048434 | Common:4; Rare:174 | ||||
| chr12:51083495-51083780 | Common:1; Rare:115 | ||||
| chr12:51172085-51172333 | Common:1; Rare:36 | ||||
| chr12:51172714-51172931 | Common:3; Rare:47 | ||||
| chr12:51173019-51173361 | Rare:67 | ||||
| chr12:51217238-51217422 | Common:1; Rare:50 | ||||
| chr12:51238584-51238951 | Common:8; Rare:143 | ||||
| chr12:51239021-51239365 | Common:3; Rare:106 | ||||
| chr12:51323927-51324249 | Rare:103 | ||||
| chr12:51391265-51391517 | Common:2; Rare:59 | ||||
| chr12:51391605-51391813 | Common:3; Rare:62 | ||||
| chr12:51392689-51392906 | Common:1; Rare:48 | ||||
| chr12:52036939-52037054 | Rare:27 | ||||
| chr12:52050966-52050996 | Common:1; Rare:4 |