| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12129412-12129737 | Rare:131 | ||||
| chr10:12195757-12196031 | Rare:67 | ||||
| chr10:12245924-12246290 | Common:1; Rare:102 | ||||
| chr10:13099766-13100234 | Common:4; Rare:118; Clinvar:3; Clinvar (benign):5 | ||||
| chr10:13300049-13300130 | Rare:31; Clinvar:1 | ||||
| chr10:13301887-13302213 | Common:1; Rare:75 | ||||
| chr10:13348003-13348334 | Rare:107 | ||||
| chr10:13348342-13348358 | Rare:5 | ||||
| chr10:14532638-14532835 | Common:2; Rare:36 | ||||
| chr10:14533080-14533211 | Rare:30 | ||||
| chr10:14604243-14604552 | Common:5; Rare:135 | ||||
| chr10:14838029-14838456 | Common:4; Rare:119 | ||||
| chr10:14878603-14878915 | Common:2; Rare:101 | ||||
| chr10:14954014-14954202 | Rare:69 | ||||
| chr10:15096997-15097253 | Common:4; Rare:96 |