| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98644986-98645296 | Common:2; Rare:92 | ||||
| chr12:100267064-100267279 | Common:1; Rare:103 | ||||
| chr12:101407731-101408056 | Common:2; Rare:81 | ||||
| chr12:102120069-102120223 | Rare:59 | ||||
| chr12:103930322-103930529 | Common:4; Rare:92 | ||||
| chr12:103942254-103942635 | Common:2; Rare:83 | ||||
| chr12:103965664-103965947 | Common:2; Rare:74 | ||||
| chr12:104064395-104064555 | Common:1; Rare:40 | ||||
| chr12:104138164-104138371 | Rare:51 | ||||
| chr12:105107612-105107789 | Common:1; Rare:80 | ||||
| chr12:105236090-105236360 | Common:2; Rare:128 | ||||
| chr12:106956657-106956781 | Rare:22 | ||||
| chr12:106987072-106987277 | Common:4; Rare:57 | ||||
| chr12:107685710-107685867 | Rare:57 | ||||
| chr12:108562439-108562658 | Common:8; Rare:96; Clinvar:2; Clinvar (benign):3 |