| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:146160270-146160590 | Common:2; Rare:56 | ||||
| chr3:146160830-146161792 | Common:8; Rare:357; Clinvar:9; Clinvar (benign):5 | ||||
| chr3:146250964-146251440 | Common:4; Rare:216 | ||||
| chr3:146468943-146470280 | Common:30; Rare:565 | ||||
| chr3:146544202-146544992 | Common:26; Rare:605 | ||||
| chr3:147393230-147393730 | Common:1; Rare:138 | ||||
| chr3:148991040-148991943 | Common:19; Rare:551; Clinvar (benign):2 | ||||
| chr3:148991921-148992640 | Common:5; Rare:373 | ||||
| chr3:149085730-149086033 | Common:6; Rare:124 | ||||
| chr3:149086030-149086390 | Common:3; Rare:135 | ||||
| chr3:149086405-149086805 | Common:4; Rare:578 | ||||
| chr3:149129300-149129720 | Common:13; Rare:488; Clinvar:10; Clinvar (benign):5 | ||||
| chr3:149129888-149130288 | Common:5; Rare:85; Clinvar:1 | ||||
| chr3:149180035-149180435 | Common:5; Rare:108 | ||||
| chr3:149576160-149576630 | Rare:111 |