| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131492519-131493223 | Common:20; Rare:339 | ||||
| chr2:131527640-131528133 | Common:11; Rare:260 | ||||
| chr2:132416210-132417036 | Common:6; Rare:411 | ||||
| chr2:132670070-132670470 | Common:4; Rare:186 | ||||
| chr2:133568098-133569100 | Common:10; Rare:317 | ||||
| chr2:134119900-134120061 | Rare:54 | ||||
| chr2:134119977-134120632 | Common:7; Rare:184 | ||||
| chr2:134718950-134719480 | Common:7; Rare:118 | ||||
| chr2:134918084-134918570 | Common:10; Rare:279 | ||||
| chr2:134918558-134918928 | Common:3; Rare:393 | ||||
| chr2:135052077-135052346 | Common:4; Rare:196; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:135052530-135052732 | Rare:62 | ||||
| chr2:135530485-135531032 | Common:8; Rare:222 | ||||
| chr2:135531127-135531681 | Common:3; Rare:305 | ||||
| chr2:135741584-135742057 | Common:9; Rare:293 |