| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:154941038-154941116 | Rare:37 | ||||
| chr5:157266016-157266177 | Rare:48 | ||||
| chr5:159263201-159263330 | Common:1; Rare:43 | ||||
| chr5:160400026-160400233 | Common:4; Rare:62 | ||||
| chr5:161546675-161547072 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr5:161848064-161848267 | Rare:37; Clinvar:2; Clinvar (benign):5 | ||||
| chr5:161848406-161848592 | Common:2; Rare:54; Clinvar (benign):3 | ||||
| chr5:162067433-162068076 | Common:2; Rare:163; Clinvar:8; Clinvar (benign):4 | ||||
| chr5:163437297-163437622 | Rare:93 | ||||
| chr5:163460048-163460157 | Common:2; Rare:46 | ||||
| chr5:169583592-169583792 | Common:6; Rare:59 | ||||
| chr5:171387501-171388004 | Rare:239; Clinvar:1 | ||||
| chr5:172454366-172454665 | Common:10; Rare:78; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172771171-172771433 | Common:4; Rare:110 | ||||
| chr5:172834163-172834402 | Common:1; Rare:58 |