| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:53946238-53946525 | Common:2; Rare:160 | ||||
| chr1:54053181-54053678 | Common:12; Rare:324 | ||||
| chr1:54199963-54200405 | Rare:248 | ||||
| chr1:54406357-54406551 | Common:6; Rare:153 | ||||
| chr1:54715726-54715905 | Common:3; Rare:57 | ||||
| chr1:54764472-54764692 | Common:5; Rare:71 | ||||
| chr1:54886989-54887450 | Common:4; Rare:257; Clinvar:9; Clinvar (benign):3 | ||||
| chr1:55039364-55039645 | Common:4; Rare:119; Clinvar:7; Clinvar (benign):2 | ||||
| chr1:55215020-55215270 | Rare:114 | ||||
| chr1:55215317-55215477 | Rare:104 | ||||
| chr1:56579103-56580100 | Common:15; Rare:329 | ||||
| chr1:56645135-56645390 | Common:1; Rare:97 | ||||
| chr1:56645560-56646200 | Common:10; Rare:208 | ||||
| chr1:58546697-58546968 | Common:4; Rare:106 | ||||
| chr1:58577240-58577456 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 |