Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209675281-209675470 | Common:1; Rare:45 | ||||
chr1:212035533-212035793 | Common:2; Rare:65 | ||||
chr1:212791766-212791926 | Common:3; Rare:62 | ||||
chr1:212858089-212858240 | Common:3; Rare:31 | ||||
chr1:214281031-214281259 | Common:2; Rare:102 | ||||
chr1:217631029-217631365 | Common:2; Rare:91 | ||||
chr1:221742072-221742325 | Common:1; Rare:75 | ||||
chr1:222589912-222589934 | Rare:4 | ||||
chr1:222712242-222712593 | Rare:109 | ||||
chr1:224175717-224175832 | Rare:38 | ||||
chr1:224330140-224330461 | Common:6; Rare:104 | ||||
chr1:225428024-225428291 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
chr1:225924236-225924441 | Common:6; Rare:55 | ||||
chr1:225999319-225999616 | Common:2; Rare:97 | ||||
chr1:227735232-227735477 | Common:3; Rare:142 |