Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:203305265-203305538 | Common:3; Rare:70 | ||||
chr1:203795467-203795729 | Common:1; Rare:80 | ||||
chr1:203861425-203861672 | Common:2; Rare:93 | ||||
chr1:204359899-204360150 | Common:1; Rare:42 | ||||
chr1:204411810-204412107 | Common:9; Rare:87 | ||||
chr1:204494751-204494955 | Rare:66 | ||||
chr1:205042996-205043262 | Common:3; Rare:58 | ||||
chr1:205121948-205122330 | Common:3; Rare:106 | ||||
chr1:205211323-205211495 | Common:2; Rare:89; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:205456029-205456068 | Rare:5 | ||||
chr1:205813125-205813491 | Common:3; Rare:148 | ||||
chr1:205943454-205943507 | Rare:10 | ||||
chr1:206003426-206003478 | Rare:11 | ||||
chr1:206612443-206612639 | Common:3; Rare:52 | ||||
chr1:207032669-207032926 | Common:3; Rare:42 |