| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:80341310-80341478 | Rare:52 | ||||
| chr13:93226791-93227539 | Common:3; Rare:171; Clinvar:8; Clinvar (benign):3 | ||||
| chr13:94601550-94601954 | Common:4; Rare:130 | ||||
| chr13:95301367-95301596 | Rare:64 | ||||
| chr13:95676894-95677236 | Common:4; Rare:125 | ||||
| chr13:96053209-96053608 | Common:3; Rare:162 | ||||
| chr13:97222194-97222485 | Rare:50 | ||||
| chr13:97976404-97976701 | Common:1; Rare:110 | ||||
| chr13:99200667-99200914 | Common:6; Rare:116 | ||||
| chr13:99307354-99307555 | Common:2; Rare:27 | ||||
| chr13:100088909-100089123 | Rare:80; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674814-100675137 | Common:4; Rare:135 | ||||
| chr13:102596794-102597059 | Common:1; Rare:123; Clinvar (benign):1 | ||||
| chr13:102773726-102773835 | Rare:53 | ||||
| chr13:102798945-102799124 | Common:1; Rare:39 |