| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:35855551-35855825 | Common:1; Rare:58 | ||||
| chr13:36346238-36346470 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346637-36346787 | Common:4; Rare:42 | ||||
| chr13:37000759-37000815 | Rare:29; Clinvar (pathogenic):1 | ||||
| chr13:37059585-37059745 | Common:1; Rare:53 | ||||
| chr13:38349793-38349910 | Common:1; Rare:58 | ||||
| chr13:38350208-38350533 | Common:2; Rare:94 | ||||
| chr13:39038064-39038426 | Common:1; Rare:92 | ||||
| chr13:39655625-39655802 | Common:2; Rare:88; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40982877-40983032 | Common:3; Rare:24 | ||||
| chr13:41019235-41019421 | Rare:29 | ||||
| chr13:41060873-41061052 | Common:16; Rare:106 | ||||
| chr13:41061144-41061587 | Common:4; Rare:148 | ||||
| chr13:41132759-41132980 | Rare:57 | ||||
| chr13:41194524-41194601 | Common:2; Rare:15 |