| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121755385-121755840 | Common:6; Rare:147 | ||||
| chr2:127294064-127294213 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387904-127388255 | Common:9; Rare:156 | ||||
| chr2:127811121-127811224 | Rare:36 | ||||
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:127885884-127886305 | Common:1; Rare:112 | ||||
| chr2:128028023-128028241 | Common:1; Rare:65 | ||||
| chr2:128091056-128091347 | Common:8; Rare:97 | ||||
| chr2:128318856-128319034 | Common:1; Rare:67 | ||||
| chr2:130181531-130181782 | Common:4; Rare:113 | ||||
| chr2:130342111-130342244 | Rare:59; Clinvar:1 | ||||
| chr2:130342686-130342932 | Common:3; Rare:80 | ||||
| chr2:130836809-130836989 | Common:2; Rare:75 | ||||
| chr2:131040009-131040390 | Rare:164 | ||||
| chr2:131093378-131093533 | Common:1; Rare:70 |