| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:53508079-53508956 | Common:15; Rare:363 | ||||
| chr4:53591333-53592070 | Common:8; Rare:259 | ||||
| chr4:54063826-54064432 | Common:10; Rare:474 | ||||
| chr4:54064494-54064894 | Common:18; Rare:517 | ||||
| chr4:54657730-54658010 | Common:4; Rare:166; Clinvar (benign):1 | ||||
| chr4:55345820-55346430 | Common:20; Rare:543; Clinvar:22; Clinvar (benign):17; Clinvar (pathogenic):1 | ||||
| chr4:55346444-55347218 | Common:8; Rare:335; Clinvar:3 | ||||
| chr4:55395360-55395722 | Common:2; Rare:167 | ||||
| chr4:55395730-55395860 | Common:5; Rare:47 | ||||
| chr4:55395790-55396108 | Common:11; Rare:339; Clinvar:12 | ||||
| chr4:55396295-55396714 | Common:12; Rare:263; Clinvar (benign):2 | ||||
| chr4:55398490-55398890 | Common:7; Rare:93 | ||||
| chr4:55398986-55399386 | Rare:75 | ||||
| chr4:55545143-55546220 | Common:20; Rare:766 | ||||
| chr4:55546322-55546780 | Common:27; Rare:512 |