| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129893558-129893911 | Rare:139 | ||||
| chr3:130746792-130746946 | Common:3; Rare:45 | ||||
| chr3:130893905-130894231 | Common:3; Rare:96 | ||||
| chr3:131026559-131026955 | Common:2; Rare:88 | ||||
| chr3:131381432-131381901 | Common:4; Rare:137 | ||||
| chr3:131502742-131503023 | Common:1; Rare:112 | ||||
| chr3:132417191-132417534 | Common:2; Rare:108 | ||||
| chr3:132659796-132659966 | Common:3; Rare:41 | ||||
| chr3:133661856-133662033 | Rare:41 | ||||
| chr3:134374373-134374695 | Common:1; Rare:93 | ||||
| chr3:134485427-134485772 | Rare:83 | ||||
| chr3:134485916-134486468 | Common:7; Rare:183 | ||||
| chr3:136196559-136196734 | Rare:51 | ||||
| chr3:136250265-136250433 | Common:2; Rare:72; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr3:136752207-136752871 | Common:2; Rare:227 |