| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119366595-119367080 | Common:3; Rare:124 | ||||
| chr2:119431646-119431862 | Common:6; Rare:56 | ||||
| chr2:119679016-119679225 | Common:3; Rare:61 | ||||
| chr2:119759739-119759872 | Common:1; Rare:36 | ||||
| chr2:120252608-120252967 | Common:3; Rare:117 | ||||
| chr2:121530554-121530889 | Common:8; Rare:140; Clinvar (pathogenic):1 | ||||
| chr2:121649394-121649645 | Common:2; Rare:75 | ||||
| chr2:121736744-121737236 | Common:5; Rare:199 | ||||
| chr2:121755379-121755788 | Common:6; Rare:133 | ||||
| chr2:124025171-124025293 | Common:2; Rare:41 | ||||
| chr2:126655917-126656214 | Common:1; Rare:68 | ||||
| chr2:127294079-127294212 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127526433-127526619 | Common:2; Rare:59 | ||||
| chr2:127811121-127811264 | Rare:45 | ||||
| chr2:127858107-127858182 | Rare:43 |