| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:10973064-10973363 | Common:3; Rare:87 | ||||
| chr7:19772223-19772552 | Common:1; Rare:64 | ||||
| chr7:25359905-25360066 | Common:2; Rare:30 | ||||
| chr7:26193249-26193692 | Rare:155; Clinvar (benign):2 | ||||
| chr7:26200137-26200210 | Rare:33 | ||||
| chr7:26376033-26376242 | Common:2; Rare:65 | ||||
| chr7:26376593-26376784 | Rare:37 | ||||
| chr7:26376956-26377247 | Common:9; Rare:51 | ||||
| chr7:26398512-26399012 | Common:7; Rare:145 | ||||
| chr7:26439843-26440124 | Rare:37 | ||||
| chr7:26440177-26440536 | Common:1; Rare:58 | ||||
| chr7:26441101-26441225 | Rare:21 | ||||
| chr7:26494025-26494070 | Rare:8 | ||||
| chr7:26655616-26655914 | Common:2; Rare:57 | ||||
| chr7:29189903-29190082 | Rare:29 |