| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47176451-47176569 | Rare:87; Clinvar (benign):5 | ||||
| chr2:47176839-47176966 | Common:3; Rare:53 | ||||
| chr2:47344993-47345355 | Common:2; Rare:96 | ||||
| chr2:47402892-47403202 | Common:1; Rare:142; Clinvar:46; Clinvar (benign):30; Clinvar (pathogenic):1 | ||||
| chr2:47570911-47571050 | Rare:41 | ||||
| chr2:47782924-47783230 | Common:2; Rare:140; Clinvar:7; Clinvar (benign):18 | ||||
| chr2:47783710-47783990 | Common:7; Rare:65; Clinvar (benign):2 | ||||
| chr2:47905719-47905911 | Rare:88 | ||||
| chr2:48314388-48314743 | Rare:128 | ||||
| chr2:48440571-48440863 | Common:9; Rare:135 | ||||
| chr2:48530030-48530197 | Common:5; Rare:84 | ||||
| chr2:49973978-49974298 | Common:2; Rare:102 | ||||
| chr2:50347500-50348060 | Common:4; Rare:134 | ||||
| chr2:51031940-51032420 | Common:2; Rare:125; Clinvar:9; Clinvar (benign):2 | ||||
| chr2:53767482-53767889 | Common:5; Rare:133 |