| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203014676-203014931 | Common:1; Rare:77 | ||||
| chr2:203238663-203239040 | Common:1; Rare:110 | ||||
| chr2:203239229-203239348 | Rare:43 | ||||
| chr2:203328200-203328400 | Common:2; Rare:78 | ||||
| chr2:206085824-206085967 | Common:1; Rare:38 | ||||
| chr2:206159370-206160036 | Common:4; Rare:202; Clinvar (benign):1 | ||||
| chr2:206765330-206765645 | Common:3; Rare:80; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:208255056-208255234 | Common:2; Rare:47 | ||||
| chr2:208266063-208266276 | Common:8; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210314898-210315272 | Common:7; Rare:110 | ||||
| chr2:214809670-214810011 | Common:1; Rare:123; Clinvar:1 | ||||
| chr2:215311993-215312081 | Common:2; Rare:37 | ||||
| chr2:216081756-216081935 | Common:1; Rare:62 | ||||
| chr2:216498740-216498887 | Common:5; Rare:60 | ||||
| chr2:216694603-216694725 | Rare:33 |