| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36876650-36876915 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877091-36877161 | Rare:29; Clinvar:1 | ||||
| chr5:37371053-37371215 | Rare:56 | ||||
| chr5:37379054-37379364 | Common:3; Rare:72 | ||||
| chr5:38557225-38557424 | Rare:53 | ||||
| chr5:38845746-38846096 | Common:2; Rare:91 | ||||
| chr5:39074333-39074539 | Common:1; Rare:103 | ||||
| chr5:39371278-39371420 | Common:2; Rare:21 | ||||
| chr5:40679728-40679938 | Common:1; Rare:43 | ||||
| chr5:40755826-40756116 | Rare:75 | ||||
| chr5:40798101-40798401 | Common:1; Rare:110 | ||||
| chr5:41904025-41904389 | Common:2; Rare:117 | ||||
| chr5:43043080-43043369 | Common:1; Rare:54 | ||||
| chr5:43064825-43065143 | Common:1; Rare:73 | ||||
| chr5:43067140-43067545 | Rare:71 |