| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135530548-135530672 | Rare:27 | ||||
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:135741591-135741965 | Common:5; Rare:132 | ||||
| chr2:135985404-135985670 | Common:4; Rare:119; Clinvar (benign):1 | ||||
| chr2:135985683-135985720 | Rare:8 | ||||
| chr2:135985862-135985976 | Common:1; Rare:27 | ||||
| chr2:136118142-136118332 | Rare:51 | ||||
| chr2:137964053-137964646 | Common:5; Rare:110 | ||||
| chr2:138501653-138502017 | Common:3; Rare:133 | ||||
| chr2:142130958-142131228 | Rare:60 | ||||
| chr2:143129043-143129439 | Common:2; Rare:86 | ||||
| chr2:144332452-144332672 | Rare:89 | ||||
| chr2:144513715-144513954 | Rare:70 | ||||
| chr2:144514308-144514579 | Common:1; Rare:38 | ||||
| chr2:144517284-144517796 | Common:7; Rare:146; Clinvar:3; Clinvar (benign):5 |