| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101815593-101815937 | Common:2; Rare:92 | ||||
| chr7:102464832-102465000 | Common:1; Rare:69 | ||||
| chr7:102671631-102671881 | Common:8; Rare:34 | ||||
| chr7:102748730-102749041 | Common:2; Rare:76 | ||||
| chr7:102749063-102749208 | Common:1; Rare:44 | ||||
| chr7:103297327-103297462 | Common:1; Rare:41 | ||||
| chr7:104207932-104208113 | Common:3; Rare:91 | ||||
| chr7:105013581-105013719 | Common:1; Rare:46 | ||||
| chr7:105014076-105014249 | Common:2; Rare:74 | ||||
| chr7:105522174-105522329 | Common:3; Rare:59 | ||||
| chr7:105532071-105532225 | Rare:43 | ||||
| chr7:105876477-105876824 | Common:6; Rare:104 | ||||
| chr7:106112161-106112577 | Common:3; Rare:149 | ||||
| chr7:106284876-106285476 | Common:6; Rare:217 | ||||
| chr7:107563846-107564032 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):4 |