| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43483765-43484008 | Common:6; Rare:138 | ||||
| chr5:43484282-43484639 | Common:1; Rare:91 | ||||
| chr5:43515016-43515330 | Common:8; Rare:192 | ||||
| chr5:43556754-43556913 | Common:5; Rare:94 | ||||
| chr5:43556829-43557187 | Common:5; Rare:172 | ||||
| chr5:43602554-43602752 | Common:2; Rare:50 | ||||
| chr5:43602850-43603291 | Rare:162 | ||||
| chr5:44808345-44809090 | Common:6; Rare:344 | ||||
| chr5:44809330-44809760 | Common:1; Rare:273 | ||||
| chr5:44809824-44809928 | Common:1; Rare:15 | ||||
| chr5:50667345-50667745 | Common:1; Rare:159 | ||||
| chr5:50667760-50667957 | Common:2; Rare:119 | ||||
| chr5:52787602-52788399 | Common:7; Rare:193 | ||||
| chr5:52989075-52989468 | Common:10; Rare:211; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:53109716-53109923 | Common:2; Rare:201; Clinvar:5 |