| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:6202752-6202940 | Common:4; Rare:50 | ||||
| chr10:7787934-7788245 | Common:1; Rare:132 | ||||
| chr10:7818409-7818520 | Common:1; Rare:25 | ||||
| chr10:11611597-11611837 | Common:2; Rare:95 | ||||
| chr10:12043197-12043365 | Common:2; Rare:49 | ||||
| chr10:12195800-12196248 | Rare:123 | ||||
| chr10:14838009-14838345 | Common:2; Rare:87 | ||||
| chr10:14878617-14878884 | Common:2; Rare:83 | ||||
| chr10:14954023-14954195 | Rare:61 | ||||
| chr10:15860464-15860583 | Rare:34 | ||||
| chr10:16817335-16817744 | Common:4; Rare:147 | ||||
| chr10:17643893-17644205 | Common:1; Rare:92 | ||||
| chr10:18651553-18651735 | Common:1; Rare:76 | ||||
| chr10:27154315-27154474 | Rare:42 | ||||
| chr10:27155212-27155386 | Common:4; Rare:63; Clinvar:2; Clinvar (benign):4 |