| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172771168-172771378 | Common:4; Rare:90 | ||||
| chr5:172834139-172834338 | Common:1; Rare:50 | ||||
| chr5:172933430-172933830 | Common:6; Rare:107 | ||||
| chr5:172959317-172959497 | Common:3; Rare:62 | ||||
| chr5:172983661-172983850 | Common:1; Rare:73 | ||||
| chr5:173056141-173056383 | Common:1; Rare:68 | ||||
| chr5:173057078-173057420 | Common:2; Rare:92 | ||||
| chr5:173144400-173144589 | Common:1; Rare:59 | ||||
| chr5:173328384-173328637 | Rare:53 | ||||
| chr5:173329337-173330121 | Common:7; Rare:285 | ||||
| chr5:173616604-173616946 | Common:1; Rare:99 | ||||
| chr5:173888013-173888374 | Rare:102 | ||||
| chr5:173917875-173918267 | Common:2; Rare:96 | ||||
| chr5:174723769-174724169 | Rare:208 | ||||
| chr5:174724186-174724751 | Common:26; Rare:393; Clinvar:4; Clinvar (benign):2 |