Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778608-778805 | Common:3; Rare:85 | ||||
chr1:827504-827676 | Common:1; Rare:70 | ||||
chr1:1064248-1064531 | Common:2; Rare:74 | ||||
chr1:9689419-9689602 | Common:1; Rare:46 | ||||
chr1:12619105-12619233 | Rare:27 | ||||
chr1:15834920-15835124 | Common:1; Rare:89 | ||||
chr1:16155034-16155248 | Common:1; Rare:43 | ||||
chr1:16644646-16644790 | Common:1; Rare:2 | ||||
chr1:17192483-17192642 | Common:1; Rare:30 | ||||
chr1:19011086-19011441 | Common:3; Rare:66 | ||||
chr1:22025202-22025522 | Common:7; Rare:77 | ||||
chr1:25875508-25875797 | Rare:79 | ||||
chr1:26865060-26865274 | Common:3; Rare:62 | ||||
chr1:28581866-28582095 | Common:2; Rare:66 | ||||
chr1:58575927-58576179 | Common:4; Rare:52; Clinvar:2; Clinvar (benign):5 |