| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47782971-47783210 | Common:2; Rare:108; Clinvar:5; Clinvar (benign):10 | ||||
| chr2:48440615-48440839 | Common:7; Rare:103 | ||||
| chr2:53786842-53787095 | Rare:90 | ||||
| chr2:53970788-53971133 | Common:10; Rare:118 | ||||
| chr2:54558182-54558428 | Common:2; Rare:81 | ||||
| chr2:55050494-55050679 | Common:2; Rare:59 | ||||
| chr2:55232241-55232426 | Common:3; Rare:44 | ||||
| chr2:55269183-55269310 | Common:2; Rare:35 | ||||
| chr2:55519421-55519870 | Common:2; Rare:148 | ||||
| chr2:55693808-55693967 | Rare:56; Clinvar (benign):2 | ||||
| chr2:58046739-58046885 | Common:2; Rare:48 | ||||
| chr2:60756080-60756312 | Rare:77 | ||||
| chr2:60881391-60881617 | Common:2; Rare:85 | ||||
| chr2:61017429-61017753 | Common:1; Rare:96; Clinvar:2 | ||||
| chr2:61065621-61065939 | Common:3; Rare:102 |