Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:202958186-202958469 | Common:3; Rare:86 | ||||
chr1:202967218-202967531 | Common:6; Rare:63 | ||||
chr1:203007234-203007435 | Common:1; Rare:76 | ||||
chr1:203305300-203305526 | Common:3; Rare:57 | ||||
chr1:203626679-203626858 | Common:1; Rare:43 | ||||
chr1:204411810-204411964 | Common:2; Rare:61 | ||||
chr1:204516288-204516481 | Common:1; Rare:57 | ||||
chr1:205121948-205122271 | Common:2; Rare:91 | ||||
chr1:207751930-207752248 | Common:1; Rare:104; Clinvar:1 | ||||
chr1:209675197-209675492 | Common:2; Rare:75 | ||||
chr1:209784521-209784697 | Rare:57 | ||||
chr1:209806137-209806309 | Common:5; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
chr1:209827853-209828059 | Common:1; Rare:55 | ||||
chr1:211259057-211259399 | Common:1; Rare:108 | ||||
chr1:211675588-211675733 | Rare:30 |