| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827450-102828308 | Common:13; Rare:507 | ||||
| chr4:102868779-102869075 | Common:4; Rare:192 | ||||
| chr4:102869120-102869546 | Common:2; Rare:211 | ||||
| chr4:103019520-103019870 | Common:3; Rare:145 | ||||
| chr4:103198332-103198681 | Common:3; Rare:86 | ||||
| chr4:105146310-105146525 | Common:2; Rare:97 | ||||
| chr4:105146744-105146928 | Common:2; Rare:79 | ||||
| chr4:105708628-105708885 | Common:5; Rare:155 | ||||
| chr4:106316132-106316621 | Common:10; Rare:278 | ||||
| chr4:107720163-107720524 | Common:13; Rare:241 | ||||
| chr4:107824400-107825090 | Common:4; Rare:302 | ||||
| chr4:107989663-107989952 | Common:12; Rare:247; Clinvar:8; Clinvar (benign):10 | ||||
| chr4:108620384-108620713 | Common:12; Rare:286 | ||||
| chr4:109302651-109303064 | Common:9; Rare:219 | ||||
| chr4:109433715-109433867 | Common:2; Rare:102 |