Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:22537352-22537650 | Common:2; Rare:44 | ||||
chr1:22634934-22635050 | Common:1; Rare:14 | ||||
chr1:23153143-23153256 | Rare:17 | ||||
chr1:23748886-23749072 | Common:1; Rare:40 | ||||
chr1:23792881-23793038 | Common:2; Rare:39 | ||||
chr1:25659100-25659120 | Rare:3 | ||||
chr1:25808762-25809057 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):5 | ||||
chr1:25875508-25875837 | Rare:88 | ||||
chr1:26282490-26282759 | Common:1; Rare:93 | ||||
chr1:26538151-26538363 | Common:3; Rare:27 | ||||
chr1:26542291-26542590 | Common:1; Rare:51 | ||||
chr1:26620908-26621100 | Rare:65 | ||||
chr1:26692377-26692628 | Common:1; Rare:55 | ||||
chr1:26697186-26697502 | Common:1; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
chr1:27031621-27031818 | Common:3; Rare:41 |