Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1876142-1876269 | Common:1; Rare:49 | ||||
chr19:2165271-2165383 | Rare:51 | ||||
chr19:2168893-2168980 | Common:1; Rare:22 | ||||
chr19:2634598-2634846 | Common:1; Rare:61 | ||||
chr19:3360680-3360787 | Rare:30 | ||||
chr19:3670337-3670395 | Rare:14 | ||||
chr19:3977213-3977612 | Common:4; Rare:130; Clinvar (benign):8 | ||||
chr19:4058416-4058592 | Common:1; Rare:51 | ||||
chr19:4504661-4505085 | Common:2; Rare:160 | ||||
chr19:4513586-4513913 | Rare:112 | ||||
chr19:4516928-4517083 | Common:2; Rare:36 | ||||
chr19:4521824-4521912 | Common:1; Rare:12 | ||||
chr19:5205862-5205979 | Rare:29 | ||||
chr19:5207959-5208158 | Rare:70 | ||||
chr19:5214560-5214858 | Common:2; Rare:105 |