| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:35476655-35476809 | Common:1; Rare:23 | ||||
| chr13:36346229-36346470 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:37000259-37000400 | Common:2; Rare:26 | ||||
| chr13:37000736-37000815 | Rare:33; Clinvar (pathogenic):1 | ||||
| chr13:37059585-37059736 | Common:1; Rare:51 | ||||
| chr13:38349548-38349916 | Common:3; Rare:125; Clinvar (pathogenic):1 | ||||
| chr13:39038086-39038468 | Common:1; Rare:92 | ||||
| chr13:41060868-41061260 | Common:17; Rare:181 | ||||
| chr13:41061352-41061675 | Common:2; Rare:103 | ||||
| chr13:41132719-41132971 | Rare:66 | ||||
| chr13:41457302-41457547 | Common:2; Rare:74 | ||||
| chr13:41960869-41961146 | Common:2; Rare:86 | ||||
| chr13:43879492-43879585 | Rare:28 | ||||
| chr13:43879718-43879894 | Common:18; Rare:56 | ||||
| chr13:44436731-44436997 | Common:2; Rare:77 |