| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:9070499-9070721 | Common:1; Rare:44 | ||||
| chr12:9072357-9072802 | Rare:102 | ||||
| chr12:9240345-9240409 | Common:1; Rare:10 | ||||
| chr12:9283905-9284046 | Common:4; Rare:7 | ||||
| chr12:9448142-9448349 | Common:2; Rare:91 | ||||
| chr12:9647972-9648375 | Common:5; Rare:127 | ||||
| chr12:9648516-9648686 | Common:2; Rare:36 | ||||
| chr12:9739866-9740007 | Common:1; Rare:52 | ||||
| chr12:10363406-10363736 | Common:4; Rare:76 | ||||
| chr12:12725088-12725400 | Common:1; Rare:85 | ||||
| chr12:12808071-12808209 | Common:1; Rare:18 | ||||
| chr12:12927525-12927770 | Common:5; Rare:75 | ||||
| chr12:14882124-14882470 | Common:5; Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:14882943-14883076 | Rare:46; Clinvar (benign):2 | ||||
| chr12:15688490-15688536 | Rare:8 |