Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:174395678-174395772 | Common:1; Rare:30 | ||||
chr2:174487072-174487385 | Common:2; Rare:66 | ||||
chr2:186485998-186486344 | Common:3; Rare:97 | ||||
chr2:189784294-189784506 | Common:3; Rare:67; Clinvar:6; Clinvar (benign):1 | ||||
chr2:191677833-191678146 | Common:4; Rare:88 | ||||
chr2:197499826-197500427 | Common:1; Rare:236; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197515876-197516089 | Common:1; Rare:83 | ||||
chr2:200889037-200889420 | Common:2; Rare:125 | ||||
chr2:201071688-201072039 | Rare:70 | ||||
chr2:201642646-201642770 | Rare:64 | ||||
chr2:203328285-203328430 | Common:1; Rare:57 | ||||
chr2:206159418-206159683 | Rare:88 | ||||
chr2:208255047-208255228 | Common:2; Rare:48 | ||||
chr2:214809639-214809991 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):2 | ||||
chr2:216498715-216498875 | Common:6; Rare:62 |