| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118088171-118088516 | Common:2; Rare:92 | ||||
| chr2:119366804-119367060 | Common:1; Rare:74 | ||||
| chr2:119678936-119679240 | Common:6; Rare:78 | ||||
| chr2:121530596-121530884 | Common:7; Rare:119 | ||||
| chr2:121649415-121649702 | Common:2; Rare:82 | ||||
| chr2:121736824-121737268 | Common:5; Rare:172 | ||||
| chr2:126655949-126656204 | Common:1; Rare:56 | ||||
| chr2:127064877-127064944 | Rare:18 | ||||
| chr2:127294096-127294246 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387928-127388202 | Common:5; Rare:117 | ||||
| chr2:127526404-127526596 | Common:2; Rare:71 | ||||
| chr2:127811139-127811259 | Rare:37 | ||||
| chr2:127858096-127858265 | Common:2; Rare:83 | ||||
| chr2:127885886-127885974 | Rare:19 | ||||
| chr2:128091046-128091343 | Common:8; Rare:99 |