| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:48440631-48440851 | Common:7; Rare:108 | ||||
| chr2:51032007-51032297 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:51032493-51032597 | Common:7; Rare:29; Clinvar:3 | ||||
| chr2:53786842-53787203 | Common:1; Rare:139 | ||||
| chr2:53970780-53971141 | Common:11; Rare:125 | ||||
| chr2:54115512-54115689 | Rare:64 | ||||
| chr2:55050333-55050784 | Common:5; Rare:136 | ||||
| chr2:55232229-55232385 | Common:3; Rare:33 | ||||
| chr2:55419794-55420113 | Common:4; Rare:130 | ||||
| chr2:55519418-55519757 | Common:1; Rare:95 | ||||
| chr2:55618893-55619062 | Common:1; Rare:32 | ||||
| chr2:60550904-60551031 | Rare:35 | ||||
| chr2:60756140-60756277 | Rare:44 | ||||
| chr2:60881300-60881664 | Common:2; Rare:136 | ||||
| chr2:61017438-61017753 | Common:1; Rare:95; Clinvar:2 |