| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188292692-188292936 | Common:1; Rare:59 | ||||
| chr2:188293000-188293090 | Rare:15 | ||||
| chr2:189062847-189063064 | Rare:49; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:189179330-189179925 | Common:1; Rare:117; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:189441021-189441511 | Common:3; Rare:155 | ||||
| chr2:189580754-189580912 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783915-189784106 | Common:4; Rare:60; Clinvar (benign):1 | ||||
| chr2:189784271-189784745 | Common:7; Rare:150; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190319719-190319974 | Common:5; Rare:95; Clinvar (benign):5 | ||||
| chr2:190343845-190343949 | Rare:20 | ||||
| chr2:190534656-190534903 | Common:1; Rare:76 | ||||
| chr2:190648778-190649119 | Common:2; Rare:117 | ||||
| chr2:191014076-191014353 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191020484-191020547 | Rare:25 | ||||
| chr2:191041738-191041945 | Common:1; Rare:27 |