| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:120252520-120252940 | Common:2; Rare:128 | ||||
| chr2:121530230-121530490 | Common:1; Rare:114 | ||||
| chr2:121530545-121530888 | Common:15; Rare:261; Clinvar (pathogenic):1 | ||||
| chr2:121649404-121649711 | Common:4; Rare:174 | ||||
| chr2:121649922-121650162 | Rare:125 | ||||
| chr2:121736799-121737294 | Common:9; Rare:288 | ||||
| chr2:121755388-121755816 | Common:10; Rare:254 | ||||
| chr2:127106981-127107406 | Common:8; Rare:242; Clinvar:15; Clinvar (benign):2 | ||||
| chr2:127294061-127294258 | Common:4; Rare:138; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:127387160-127387560 | Common:10; Rare:233 | ||||
| chr2:127387881-127388260 | Common:19; Rare:309 | ||||
| chr2:127525950-127526360 | Common:3; Rare:131 | ||||
| chr2:127526421-127526596 | Common:4; Rare:107 | ||||
| chr2:127526740-127527030 | Common:1; Rare:57 | ||||
| chr2:127811149-127811298 | Common:2; Rare:92 |