| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:97971960-97972108 | Rare:45 | ||||
| chr3:97972393-97972544 | Common:5; Rare:96 | ||||
| chr3:98522040-98522500 | Common:1; Rare:191 | ||||
| chr3:98522439-98523301 | Common:13; Rare:828 | ||||
| chr3:98585410-98585810 | Common:4; Rare:165; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:98593547-98594076 | Common:10; Rare:420; Clinvar (benign):3 | ||||
| chr3:98901015-98901547 | Common:16; Rare:392 | ||||
| chr3:98901574-98902151 | Common:8; Rare:1007 | ||||
| chr3:99817533-99817935 | Common:2; Rare:849 | ||||
| chr3:99817938-99818338 | Common:3; Rare:150 | ||||
| chr3:99875534-99875934 | Common:1; Rare:75 | ||||
| chr3:99876026-99876438 | Common:13; Rare:583 | ||||
| chr3:99876543-99876978 | Common:2; Rare:147 | ||||
| chr3:100260196-100260596 | Rare:72 | ||||
| chr3:100260600-100261074 | Rare:712 |