| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121399610-121400224 | Common:37; Rare:978 | ||||
| chr12:121536065-121536946 | Common:7; Rare:313 | ||||
| chr12:121536928-121537410 | Common:7; Rare:209 | ||||
| chr12:121578970-121579420 | Common:2; Rare:92 | ||||
| chr12:121579457-121579814 | Common:2; Rare:164 | ||||
| chr12:121580010-121581450 | Common:10; Rare:973; Clinvar:2 | ||||
| chr12:121581423-121581677 | Rare:64 | ||||
| chr12:121626164-121627048 | Common:21; Rare:1115; Clinvar:16; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr12:121711940-121712351 | Common:2; Rare:234 | ||||
| chr12:121712519-121712955 | Common:29; Rare:718 | ||||
| chr12:121742873-121743661 | Common:9; Rare:166 | ||||
| chr12:121793481-121794818 | Common:22; Rare:1111 | ||||
| chr12:121799940-121800416 | Common:16; Rare:580 | ||||
| chr12:121800429-121800846 | Common:6; Rare:346 | ||||
| chr12:121800910-121801908 | Common:13; Rare:476 |