Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:94745163-94745276 | Rare:14 | ||||
chr11:94974813-94974936 | Rare:21 | ||||
chr11:94975025-94975060 | Rare:7 | ||||
chr11:95037764-95037918 | Common:2; Rare:43 | ||||
chr11:95136086-95136238 | Common:1; Rare:28 | ||||
chr11:95150879-95151200 | Common:1; Rare:75 | ||||
chr11:95482104-95482417 | Common:3; Rare:82 | ||||
chr11:95849801-95850067 | Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr11:96244258-96244369 | Rare:24 | ||||
chr11:96341778-96341918 | Common:1; Rare:42 | ||||
chr11:96341970-96342033 | Rare:5 | ||||
chr11:96449649-96449772 | Common:1; Rare:16 | ||||
chr11:96506788-96507168 | Common:5; Rare:65 | ||||
chr11:96643288-96643424 | Common:3; Rare:33 | ||||
chr11:97667548-97667883 | Common:2; Rare:94 |