| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186485983-186486451 | Common:3; Rare:135 | ||||
| chr2:186589872-186590335 | Rare:141 | ||||
| chr2:186693888-186694132 | Rare:96 | ||||
| chr2:188291595-188291791 | Common:3; Rare:47 | ||||
| chr2:188291800-188292171 | Common:4; Rare:110 | ||||
| chr2:188292692-188292948 | Common:1; Rare:59 | ||||
| chr2:188293005-188293105 | Rare:18 | ||||
| chr2:189441046-189441519 | Common:3; Rare:153 | ||||
| chr2:189580764-189580944 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189661264-189661580 | Common:5; Rare:105 | ||||
| chr2:189763186-189763237 | Rare:7 | ||||
| chr2:189783939-189784104 | Common:4; Rare:57; Clinvar (benign):1 | ||||
| chr2:189784281-189784560 | Common:4; Rare:98; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190319738-190320105 | Common:5; Rare:119; Clinvar (benign):5 | ||||
| chr2:190534656-190534913 | Common:1; Rare:81 |