| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121736745-121737098 | Common:4; Rare:143 | ||||
| chr2:121755358-121755716 | Common:3; Rare:113 | ||||
| chr2:126656038-126656306 | Common:1; Rare:78; Clinvar:2 | ||||
| chr2:127294083-127294214 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387904-127388240 | Common:8; Rare:149 | ||||
| chr2:127526421-127526598 | Common:2; Rare:59 | ||||
| chr2:127811084-127811224 | Rare:46 | ||||
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:127885886-127886504 | Common:2; Rare:168 | ||||
| chr2:128091039-128091335 | Common:8; Rare:99 | ||||
| chr2:130181571-130181797 | Common:3; Rare:96 | ||||
| chr2:130182091-130182318 | Common:2; Rare:85 | ||||
| chr2:130342122-130342279 | Rare:65; Clinvar:1 | ||||
| chr2:130342642-130342946 | Common:5; Rare:100 | ||||
| chr2:130355929-130356128 | Common:3; Rare:56 |