| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131710839-131711102 | Rare:62 | ||||
| chr12:131828076-131828457 | Common:5; Rare:121 | ||||
| chr12:131894296-131894746 | Common:3; Rare:141 | ||||
| chr12:131929050-131929200 | Common:10; Rare:41 | ||||
| chr12:131929204-131929766 | Common:1; Rare:168; Clinvar:5; Clinvar (benign):4 | ||||
| chr12:132144302-132144530 | Common:1; Rare:94 | ||||
| chr12:132275201-132275438 | Common:4; Rare:53 | ||||
| chr12:132559824-132560140 | Rare:93 | ||||
| chr12:132687285-132687663 | Common:3; Rare:137; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710736-132710877 | Common:3; Rare:60 | ||||
| chr12:132761755-132761930 | Common:3; Rare:58 | ||||
| chr12:132887470-132887825 | Common:1; Rare:113 | ||||
| chr12:132956243-132956434 | Common:1; Rare:42 | ||||
| chr12:132986236-132986428 | Rare:40 | ||||
| chr12:133037242-133037611 | Common:3; Rare:92 |