| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121736723-121737229 | Common:5; Rare:205 | ||||
| chr2:126656079-126656272 | Rare:62 | ||||
| chr2:127294077-127294235 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387956-127388255 | Common:7; Rare:130 | ||||
| chr2:127526429-127526619 | Common:2; Rare:61 | ||||
| chr2:127811121-127811259 | Rare:45 | ||||
| chr2:127885861-127885991 | Rare:32 | ||||
| chr2:128091031-128091354 | Common:8; Rare:105 | ||||
| chr2:130129304-130129631 | Common:4; Rare:98 | ||||
| chr2:130181546-130181696 | Common:1; Rare:53 | ||||
| chr2:130182072-130182447 | Common:2; Rare:137 | ||||
| chr2:130342123-130342244 | Rare:51; Clinvar:1 | ||||
| chr2:130342642-130342930 | Common:5; Rare:90 | ||||
| chr2:130836803-130836944 | Common:2; Rare:64 | ||||
| chr2:131093378-131093569 | Common:1; Rare:87 |