| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1210312-1210592 | Rare:75 | ||||
| chr5:8457595-8457751 | Common:2; Rare:46 | ||||
| chr5:9409587-9409768 | Rare:24 | ||||
| chr5:14209714-14210015 | Common:1; Rare:60 | ||||
| chr5:14701972-14702001 | Rare:5 | ||||
| chr5:14712953-14713270 | Rare:98; Clinvar (benign):2 | ||||
| chr5:16465165-16465220 | Rare:15 | ||||
| chr5:23951307-23951372 | Rare:27 | ||||
| chr5:33161905-33162164 | Common:4; Rare:43 | ||||
| chr5:40696630-40696945 | Common:1; Rare:45 | ||||
| chr5:42837149-42837186 | Rare:11 | ||||
| chr5:43065989-43066073 | Common:1; Rare:10 | ||||
| chr5:43066089-43066547 | Common:4; Rare:120 | ||||
| chr5:43066963-43067040 | Rare:19 | ||||
| chr5:55446355-55446472 | Rare:18 |