| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119760046-119760217 | Common:1; Rare:37 | ||||
| chr2:120012756-120013145 | Common:4; Rare:147 | ||||
| chr2:120252591-120252973 | Common:3; Rare:124 | ||||
| chr2:121530579-121530884 | Common:7; Rare:127 | ||||
| chr2:121649176-121649302 | Rare:23 | ||||
| chr2:121649418-121649754 | Common:2; Rare:97 | ||||
| chr2:121649911-121650151 | Common:1; Rare:62 | ||||
| chr2:121736716-121737236 | Common:5; Rare:208 | ||||
| chr2:121755392-121755774 | Common:6; Rare:127 | ||||
| chr2:126655947-126656289 | Common:1; Rare:85; Clinvar:1 | ||||
| chr2:127106954-127107366 | Common:5; Rare:123; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:127294083-127294256 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387941-127388255 | Common:8; Rare:135 | ||||
| chr2:127526410-127526595 | Common:2; Rare:67 | ||||
| chr2:127811093-127811264 | Rare:53 |