Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:97589703-97589909 | Common:6; Rare:58 | ||||
chr2:97645803-97646186 | Common:3; Rare:115 | ||||
chr2:97646770-97647099 | Common:1; Rare:82 | ||||
chr2:97663902-97664302 | Common:1; Rare:123 | ||||
chr2:98444742-98445061 | Common:1; Rare:120 | ||||
chr2:98608381-98608690 | Common:1; Rare:125; Clinvar (benign):1 | ||||
chr2:98869247-98869416 | Common:1; Rare:40 | ||||
chr2:99141119-99141619 | Common:2; Rare:197 | ||||
chr2:99141631-99141811 | Common:1; Rare:41 | ||||
chr2:99154839-99155057 | Common:2; Rare:90; Clinvar (benign):2 | ||||
chr2:99180967-99181234 | Common:2; Rare:79 | ||||
chr2:99337253-99337557 | Rare:112 | ||||
chr2:100322412-100322537 | Common:2; Rare:28 | ||||
chr2:100417389-100417697 | Rare:92 | ||||
chr2:100562663-100563054 | Common:4; Rare:119 |