| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:148883062-148883464 | Common:4; Rare:257 | ||||
| chr7:148884156-148884550 | Common:2; Rare:183; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:149028461-149029046 | Common:7; Rare:200 | ||||
| chr7:149090659-149090940 | Rare:79 | ||||
| chr7:149125500-149126080 | Common:5; Rare:245 | ||||
| chr7:149126271-149126629 | Common:9; Rare:98 | ||||
| chr7:149147150-149147590 | Common:5; Rare:97 | ||||
| chr7:149147856-149148640 | Common:4; Rare:265 | ||||
| chr7:149195353-149195526 | Rare:37 | ||||
| chr7:149206521-149206921 | Common:3; Rare:120 | ||||
| chr7:149239498-149239721 | Common:2; Rare:59 | ||||
| chr7:149261891-149262221 | Common:2; Rare:108 | ||||
| chr7:149262480-149262880 | Common:5; Rare:136 | ||||
| chr7:149460584-149460748 | Rare:32 | ||||
| chr7:149460770-149461280 | Common:1; Rare:88 |