| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:80047305-80047427 | Common:1; Rare:19 | ||||
| chr2:81466949-81467011 | Rare:10 | ||||
| chr2:81467437-81467475 | Rare:5 | ||||
| chr2:81481686-81481764 | Common:2; Rare:18 | ||||
| chr2:81868513-81868664 | Common:1; Rare:26 | ||||
| chr2:82325691-82325872 | Common:2; Rare:52 | ||||
| chr2:82326473-82326593 | Common:2; Rare:54 | ||||
| chr2:82937900-82938216 | Common:5; Rare:85 | ||||
| chr2:83245524-83245616 | Rare:17 | ||||
| chr2:85043382-85043665 | Rare:43 | ||||
| chr2:85190295-85190301 | Rare:1 | ||||
| chr2:85235007-85235322 | Common:2; Rare:43 | ||||
| chr2:85243748-85243867 | Common:2; Rare:22 | ||||
| chr2:85537885-85538021 | Rare:39 | ||||
| chr2:85542712-85542996 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):6 |