Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19033484-19033649 | Common:2; Rare:51 | ||||
chr19:19192122-19192262 | Common:1; Rare:44 | ||||
chr19:19320483-19320850 | Common:4; Rare:130 | ||||
chr19:19516163-19516287 | Rare:77; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr19:21836156-21836309 | Rare:57 | ||||
chr19:29606191-29606317 | Rare:41 | ||||
chr19:32971939-32972309 | Common:5; Rare:103 | ||||
chr19:33373566-33373821 | Common:2; Rare:79 | ||||
chr19:33521765-33521949 | Rare:55; Clinvar:3 | ||||
chr19:34677503-34677758 | Common:7; Rare:74 | ||||
chr19:35155120-35155230 | Rare:22 | ||||
chr19:35545498-35545686 | Common:4; Rare:60 | ||||
chr19:35628795-35629103 | Common:4; Rare:95 | ||||
chr19:35745352-35745681 | Rare:103 | ||||
chr19:36014214-36014515 | Common:2; Rare:82 |