| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36066031-36066332 | Rare:62 | ||||
| chr22:36332757-36332973 | Common:1; Rare:35 | ||||
| chr22:36348720-36349590 | Common:16; Rare:352; Clinvar:10; Clinvar (benign):17; Clinvar (pathogenic):2 | ||||
| chr22:36352050-36352380 | Common:6; Rare:111 | ||||
| chr22:36363459-36363935 | Common:3; Rare:115 | ||||
| chr22:36386158-36386395 | Common:2; Rare:40 | ||||
| chr22:36395020-36395460 | Common:2; Rare:77 | ||||
| chr22:36410013-36410470 | Common:14; Rare:246 | ||||
| chr22:36419241-36419641 | Common:9; Rare:98 | ||||
| chr22:36433320-36433599 | Common:2; Rare:96 | ||||
| chr22:36448946-36449370 | Common:2; Rare:70 | ||||
| chr22:36451690-36452110 | Common:2; Rare:167 | ||||
| chr22:36454912-36455431 | Common:12; Rare:357 | ||||
| chr22:36455620-36456000 | Common:2; Rare:83 | ||||
| chr22:36459420-36459935 | Common:21; Rare:225 |