| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119431709-119431877 | Common:4; Rare:42 | ||||
| chr2:119759740-119759817 | Common:1; Rare:16 | ||||
| chr2:121530609-121530895 | Common:7; Rare:130; Clinvar (pathogenic):2 | ||||
| chr2:121649418-121649703 | Common:2; Rare:82 | ||||
| chr2:121736744-121737083 | Common:2; Rare:137 | ||||
| chr2:121755415-121755718 | Common:2; Rare:97 | ||||
| chr2:126656222-126656289 | Rare:17; Clinvar:1 | ||||
| chr2:127294079-127294212 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387949-127388256 | Common:7; Rare:131 | ||||
| chr2:127681493-127681671 | Common:1; Rare:40 | ||||
| chr2:127858107-127858219 | Common:1; Rare:56 | ||||
| chr2:127885878-127885982 | Rare:25 | ||||
| chr2:128090994-128091347 | Common:8; Rare:125 | ||||
| chr2:130181553-130181775 | Common:2; Rare:99 | ||||
| chr2:130182101-130182347 | Common:2; Rare:97 |