| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119366742-119367054 | Common:1; Rare:92 | ||||
| chr2:119431573-119431877 | Common:9; Rare:73 | ||||
| chr2:119678956-119679225 | Common:5; Rare:73 | ||||
| chr2:119759715-119759821 | Common:1; Rare:24 | ||||
| chr2:120252618-120252967 | Common:3; Rare:115 | ||||
| chr2:120736082-120736156 | Rare:18 | ||||
| chr2:121530579-121530884 | Common:7; Rare:127 | ||||
| chr2:121649418-121649748 | Common:2; Rare:97 | ||||
| chr2:121649817-121650138 | Common:1; Rare:80 | ||||
| chr2:121736716-121737099 | Common:4; Rare:154 | ||||
| chr2:121755402-121755788 | Common:6; Rare:127 | ||||
| chr2:126656014-126656311 | Common:1; Rare:90; Clinvar:2 | ||||
| chr2:127294077-127294196 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387904-127388231 | Common:7; Rare:147 | ||||
| chr2:127526410-127526607 | Common:2; Rare:72 |