| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121649424-121649645 | Common:2; Rare:65 | ||||
| chr2:121736766-121737255 | Common:5; Rare:193 | ||||
| chr2:127294091-127294199 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127811139-127811254 | Rare:34 | ||||
| chr2:127885884-127885982 | Rare:24 | ||||
| chr2:128091102-128091335 | Common:5; Rare:72 | ||||
| chr2:130181553-130181777 | Common:3; Rare:99 | ||||
| chr2:130182091-130182336 | Common:2; Rare:95 | ||||
| chr2:130342094-130342228 | Rare:58; Clinvar:1 | ||||
| chr2:130342686-130342923 | Common:2; Rare:75 | ||||
| chr2:131492339-131492556 | Common:8; Rare:86 | ||||
| chr2:131493034-131493097 | Common:1; Rare:16 | ||||
| chr2:134918585-134918880 | Common:1; Rare:124 | ||||
| chr2:135531158-135531520 | Common:1; Rare:79 | ||||
| chr2:135741710-135741945 | Common:1; Rare:92 |