| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12663228-12663628 | Common:3; Rare:112 | ||||
| chr3:12663820-12663950 | Rare:41; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:12664030-12664430 | Common:15; Rare:585; Clinvar:7; Clinvar (benign):26 | ||||
| chr3:12664455-12664855 | Common:2; Rare:80 | ||||
| chr3:12768814-12769027 | Common:26; Rare:116 | ||||
| chr3:12796460-12797310 | Common:38; Rare:542 | ||||
| chr3:12840295-12841269 | Common:8; Rare:341 | ||||
| chr3:12841433-12842030 | Common:7; Rare:601 | ||||
| chr3:12966860-12967394 | Common:5; Rare:138 | ||||
| chr3:12967600-12968040 | Common:23; Rare:700 | ||||
| chr3:12994403-12994890 | Common:1; Rare:140 | ||||
| chr3:12994850-12995370 | Common:5; Rare:436 | ||||
| chr3:13419590-13419930 | Common:11; Rare:248 | ||||
| chr3:13419860-13420050 | Common:3; Rare:70 | ||||
| chr3:13420118-13420902 | Common:13; Rare:659 |