| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185143145-185143290 | Common:2; Rare:45; Clinvar (benign):3 | ||||
| chr4:185396563-185396843 | Rare:90 | ||||
| chr4:185396984-185397233 | Rare:89 | ||||
| chr4:185425880-185426278 | Common:4; Rare:118 | ||||
| chr4:185811075-185811339 | Common:1; Rare:53 | ||||
| chr4:186723674-186723946 | Common:5; Rare:102 | ||||
| chr4:189940572-189941000 | Common:15; Rare:140 | ||||
| chr5:218117-218395 | Common:3; Rare:116; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:443084-443266 | Common:9; Rare:82 | ||||
| chr5:612203-612357 | Rare:61 | ||||
| chr5:892625-892923 | Common:5; Rare:101 | ||||
| chr5:1799785-1799993 | Common:7; Rare:98 | ||||
| chr5:1801287-1801509 | Common:4; Rare:118; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:5140080-5140300 | Common:4; Rare:60 | ||||
| chr5:5422292-5422689 | Common:3; Rare:138 |