| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120437921-120438241 | Common:2; Rare:123; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446340-120446485 | Common:1; Rare:67 | ||||
| chr12:120469589-120470066 | Common:4; Rare:149 | ||||
| chr12:120495843-120496562 | Common:8; Rare:236 | ||||
| chr12:120497806-120498179 | Rare:75 | ||||
| chr12:120529093-120529243 | Common:2; Rare:55 | ||||
| chr12:120534308-120534363 | Rare:23 | ||||
| chr12:120534462-120534557 | Common:1; Rare:25 | ||||
| chr12:120581324-120581566 | Common:1; Rare:86 | ||||
| chr12:120686386-120686587 | Common:2; Rare:55 | ||||
| chr12:120686960-120687171 | Common:1; Rare:73 | ||||
| chr12:120687366-120687503 | Rare:40 | ||||
| chr12:120710208-120710477 | Common:4; Rare:69 | ||||
| chr12:120725688-120725882 | Common:2; Rare:60; Clinvar:1 | ||||
| chr12:120904373-120904735 | Rare:110 |