| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97663919-97664261 | Common:1; Rare:105 | ||||
| chr2:98608388-98608682 | Common:1; Rare:120; Clinvar (benign):1 | ||||
| chr2:99141141-99141730 | Common:3; Rare:216 | ||||
| chr2:99154877-99155079 | Common:2; Rare:79; Clinvar (benign):3 | ||||
| chr2:99180979-99181239 | Common:2; Rare:73 | ||||
| chr2:99337253-99337480 | Rare:83 | ||||
| chr2:100562731-100562817 | Rare:22 | ||||
| chr2:100562903-100563056 | Rare:52 | ||||
| chr2:101002142-101002324 | Rare:70 | ||||
| chr2:101252650-101252933 | Common:5; Rare:97 | ||||
| chr2:101308669-101308776 | Rare:46 | ||||
| chr2:101998823-101998993 | Common:1; Rare:16 | ||||
| chr2:102070278-102070476 | Common:2; Rare:35 | ||||
| chr2:102142574-102142866 | Common:1; Rare:92 | ||||
| chr2:102736817-102736980 | Common:1; Rare:77 |