Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:219210151-219210357 | Common:1; Rare:33 | ||||
chr1:220046349-220046742 | Common:1; Rare:127 | ||||
chr1:220093968-220094482 | Common:4; Rare:166; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:220272299-220272602 | Rare:91; Clinvar:5 | ||||
chr1:221742072-221742325 | Common:1; Rare:75 | ||||
chr1:222589746-222589994 | Common:2; Rare:67 | ||||
chr1:222617807-222618166 | Common:3; Rare:94 | ||||
chr1:222644087-222644437 | Common:3; Rare:106 | ||||
chr1:222712412-222712881 | Common:3; Rare:157 | ||||
chr1:222713230-222713466 | Common:1; Rare:73 | ||||
chr1:222928266-222928562 | Rare:51 | ||||
chr1:223845792-223846086 | Rare:96 | ||||
chr1:224114013-224114152 | Common:1; Rare:54 | ||||
chr1:224183122-224183417 | Common:2; Rare:109 | ||||
chr1:224330079-224330442 | Common:7; Rare:125 |