| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13300009-13300141 | Rare:52; Clinvar:2 | ||||
| chr10:13707157-13707503 | Common:3; Rare:76 | ||||
| chr10:14008157-14008228 | Rare:29 | ||||
| chr10:14838007-14838389 | Common:2; Rare:109 | ||||
| chr10:14878606-14878894 | Common:2; Rare:91 | ||||
| chr10:14954023-14954160 | Rare:44 | ||||
| chr10:15097301-15097401 | Common:1; Rare:50 | ||||
| chr10:15860432-15860583 | Rare:43 | ||||
| chr10:16817313-16817734 | Common:5; Rare:147 | ||||
| chr10:17228923-17229343 | Common:3; Rare:88 | ||||
| chr10:17230554-17230715 | Rare:69; Clinvar:1 | ||||
| chr10:17643871-17644276 | Common:2; Rare:122 | ||||
| chr10:18140487-18140862 | Common:2; Rare:130; Clinvar:5; Clinvar (benign):9 | ||||
| chr10:18141122-18141159 | Rare:10 | ||||
| chr10:18340572-18340842 | Common:3; Rare:55; Clinvar:1; Clinvar (benign):2 |