| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:157257903-157258443 | Common:2; Rare:144 | ||||
| chr2:157876306-157876666 | Rare:95 | ||||
| chr2:158968451-158968710 | Rare:83 | ||||
| chr2:159135393-159135711 | Common:3; Rare:73 | ||||
| chr2:159136009-159136295 | Common:15; Rare:107 | ||||
| chr2:159286587-159286875 | Common:4; Rare:103 | ||||
| chr2:159516521-159516650 | Common:1; Rare:15 | ||||
| chr2:159615225-159615314 | Common:2; Rare:20 | ||||
| chr2:159616409-159616695 | Common:2; Rare:56 | ||||
| chr2:159712398-159712641 | Common:2; Rare:92 | ||||
| chr2:161308351-161308722 | Common:2; Rare:83 | ||||
| chr2:162318656-162318813 | Rare:31 | ||||
| chr2:162344243-162344425 | Common:1; Rare:73 | ||||
| chr2:163735987-163736102 | Rare:22 | ||||
| chr2:166375912-166376099 | Common:4; Rare:57; Clinvar:1; Clinvar (benign):5 |