Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156591549-156591824 | Common:5; Rare:108 | ||||
chr1:156601416-156601513 | Common:1; Rare:38 | ||||
chr1:156728385-156728461 | Rare:16 | ||||
chr1:157993276-157993677 | Common:2; Rare:91 | ||||
chr1:159925456-159925617 | Common:1; Rare:42 | ||||
chr1:160343200-160343390 | Rare:77 | ||||
chr1:161045888-161046064 | Common:1; Rare:46 | ||||
chr1:161098281-161098395 | Common:1; Rare:18 | ||||
chr1:161118000-161118141 | Rare:73 | ||||
chr1:161132444-161132628 | Common:1; Rare:67 | ||||
chr1:161314268-161314399 | Common:3; Rare:45; Clinvar (benign):2 | ||||
chr1:162497761-162497864 | Common:1; Rare:37 | ||||
chr1:163321731-163322079 | Common:1; Rare:93 | ||||
chr1:165768796-165769055 | Common:2; Rare:113 | ||||
chr1:166839322-166839518 | Rare:54 |