| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:119178571-119178950 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:119178978-119179024 | Rare:6; Clinvar:1 | ||||
| chr12:119334571-119334751 | Common:1; Rare:35 | ||||
| chr12:119668105-119668229 | Common:1; Rare:28 | ||||
| chr12:119877267-119877565 | Common:2; Rare:66 | ||||
| chr12:120116712-120116970 | Common:4; Rare:96 | ||||
| chr12:120194683-120194787 | Rare:37 | ||||
| chr12:120201072-120201366 | Common:2; Rare:93 | ||||
| chr12:120265669-120266031 | Common:1; Rare:117 | ||||
| chr12:120437853-120438294 | Common:3; Rare:160; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446333-120446495 | Common:2; Rare:74 | ||||
| chr12:120469618-120469918 | Common:3; Rare:106 | ||||
| chr12:120495843-120496228 | Common:8; Rare:128 | ||||
| chr12:120529113-120529250 | Common:2; Rare:47 | ||||
| chr12:120581330-120581586 | Common:1; Rare:87 |