| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97645780-97646186 | Common:3; Rare:121 | ||||
| chr2:97663912-97664261 | Common:1; Rare:106 | ||||
| chr2:98608425-98608665 | Common:1; Rare:105; Clinvar (benign):1 | ||||
| chr2:99141141-99141259 | Common:1; Rare:44 | ||||
| chr2:99141512-99141749 | Common:2; Rare:88 | ||||
| chr2:99154845-99155054 | Common:2; Rare:88; Clinvar (benign):2 | ||||
| chr2:99180979-99181243 | Common:2; Rare:75 | ||||
| chr2:100417389-100417705 | Rare:93 | ||||
| chr2:100562635-100563054 | Common:5; Rare:124 | ||||
| chr2:101002123-101002318 | Rare:73 | ||||
| chr2:102736856-102736949 | Common:1; Rare:34 | ||||
| chr2:105037884-105038117 | Common:3; Rare:84 | ||||
| chr2:105337211-105337606 | Common:5; Rare:140 | ||||
| chr2:105398991-105399273 | Common:1; Rare:99 | ||||
| chr2:106194237-106194543 | Common:6; Rare:129 |