Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:34205485-34205789 | Common:1; Rare:46 | ||||
chr19:34414506-34414545 | Rare:1 | ||||
chr19:34683527-34683643 | Common:2; Rare:18 | ||||
chr19:35021763-35022039 | Common:2; Rare:107 | ||||
chr19:35061913-35062224 | Common:3; Rare:48 | ||||
chr19:35091040-35091076 | Rare:6 | ||||
chr19:35158369-35158538 | Common:5; Rare:37 | ||||
chr19:35384231-35384289 | Common:2; Rare:9 | ||||
chr19:35542659-35542947 | Common:1; Rare:54 | ||||
chr19:35673268-35673374 | Rare:40 | ||||
chr19:35936241-35936374 | Common:1; Rare:29 | ||||
chr19:36003489-36003641 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
chr19:36017408-36017678 | Common:1; Rare:77 | ||||
chr19:36145974-36146303 | Common:1; Rare:102 | ||||
chr19:36315214-36315521 | Common:4; Rare:33 |