Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:215567479-215567687 | Rare:65 | ||||
chr1:217630988-217631375 | Common:2; Rare:111 | ||||
chr1:218285178-218285452 | Common:4; Rare:113 | ||||
chr1:219173766-219173902 | Common:1; Rare:73 | ||||
chr1:220272320-220272548 | Rare:70; Clinvar:5 | ||||
chr1:221741835-221742288 | Common:1; Rare:112 | ||||
chr1:222589774-222589978 | Common:2; Rare:59 | ||||
chr1:222617792-222618143 | Common:3; Rare:89 | ||||
chr1:222644022-222644419 | Common:3; Rare:121 | ||||
chr1:222712455-222712917 | Common:3; Rare:157 | ||||
chr1:222713243-222713416 | Common:1; Rare:53 | ||||
chr1:223143218-223143373 | Common:3; Rare:43 | ||||
chr1:224114039-224114141 | Common:1; Rare:42 | ||||
chr1:224330131-224330442 | Common:7; Rare:94 | ||||
chr1:225427994-225428280 | Common:3; Rare:90; Clinvar:3; Clinvar (benign):2 |