| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118013963-118014229 | Common:3; Rare:133 | ||||
| chr2:118088382-118088591 | Rare:51 | ||||
| chr2:119366731-119367063 | Common:1; Rare:95 | ||||
| chr2:119367180-119367284 | Rare:21 | ||||
| chr2:119759758-119760143 | Common:3; Rare:101 | ||||
| chr2:120735824-120736232 | Common:2; Rare:118 | ||||
| chr2:121530564-121530897 | Common:7; Rare:150; Clinvar (pathogenic):3 | ||||
| chr2:121649419-121649666 | Common:2; Rare:70 | ||||
| chr2:121736757-121737111 | Common:4; Rare:143 | ||||
| chr2:121755402-121755866 | Common:6; Rare:152 | ||||
| chr2:126656018-126656330 | Common:1; Rare:100; Clinvar:2 | ||||
| chr2:127106862-127107115 | Common:1; Rare:71; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:127294091-127294238 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387941-127388248 | Common:8; Rare:132 | ||||
| chr2:127526404-127526599 | Common:2; Rare:72 |