Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7857382-7858125 | Common:5; Rare:248 | ||||
chr17:7931898-7932253 | Common:5; Rare:96 | ||||
chr17:10697505-10697616 | Common:2; Rare:42; Clinvar:2; Clinvar (benign):2 | ||||
chr17:11997431-11997586 | Rare:54 | ||||
chr17:14069430-14069559 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15260751-15260896 | Rare:61; Clinvar (benign):2 | ||||
chr17:15262470-15262699 | Rare:54 | ||||
chr17:15999568-15999851 | Common:3; Rare:145; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:17237101-17237430 | Common:4; Rare:102; Clinvar:1; Clinvar (benign):3 | ||||
chr17:18039079-18039420 | Common:4; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
chr17:18184735-18184877 | Common:1; Rare:32 | ||||
chr17:18314928-18315337 | Common:1; Rare:120 | ||||
chr17:18781117-18781304 | Common:3; Rare:51 | ||||
chr17:19377892-19378035 | Common:1; Rare:35 | ||||
chr17:19378134-19378578 | Common:2; Rare:104 |