| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185396468-185396845 | Rare:125 | ||||
| chr4:185397029-185397246 | Rare:79 | ||||
| chr4:185425870-185426263 | Common:4; Rare:119 | ||||
| chr4:185535504-185535635 | Rare:30 | ||||
| chr4:186723756-186723921 | Common:5; Rare:68 | ||||
| chr4:186726620-186726788 | Common:4; Rare:54 | ||||
| chr4:188109353-188109438 | Rare:23 | ||||
| chr4:189940620-189941066 | Common:16; Rare:166 | ||||
| chr5:218094-218414 | Common:4; Rare:128; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:271793-272089 | Common:3; Rare:103 | ||||
| chr5:443068-443288 | Common:10; Rare:103 | ||||
| chr5:612191-612381 | Rare:80 | ||||
| chr5:693312-693551 | Common:6; Rare:68 | ||||
| chr5:891531-891686 | Rare:44 | ||||
| chr5:892363-893087 | Common:6; Rare:224 |