Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:13749191-13749455 | Common:2; Rare:96 | ||||
chr1:15526553-15526905 | Common:2; Rare:112 | ||||
chr1:16613525-16613665 | |||||
chr1:17054076-17054362 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
chr1:17439662-17439887 | Rare:72 | ||||
chr1:18480866-18481026 | Common:1; Rare:33 | ||||
chr1:19210091-19210404 | Rare:112 | ||||
chr1:19251480-19251842 | Common:6; Rare:126 | ||||
chr1:19311970-19312343 | Common:8; Rare:170 | ||||
chr1:19485460-19485775 | Rare:119 | ||||
chr1:19596667-19597064 | Common:3; Rare:130 | ||||
chr1:20508079-20508314 | Common:5; Rare:72 | ||||
chr1:20661331-20661699 | Common:3; Rare:133; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786642-20786870 | Rare:89 | ||||
chr1:20787259-20787493 | Rare:109 |