Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:218402634-218402714 | Rare:25 | ||||
chr2:237326442-237326760 | Rare:56 | ||||
chr2:237359034-237359250 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:238883420-238883445 | Rare:5 | ||||
chr2:240456692-240456797 | Rare:26 | ||||
chr2:241882369-241882450 | Rare:23 | ||||
chr20:2796392-2796611 | Common:1; Rare:55 | ||||
chr20:3749731-3749763 | Rare:14 | ||||
chr20:17621470-17621732 | Common:3; Rare:83 | ||||
chr20:18793982-18794089 | Rare:33 | ||||
chr20:19757959-19758270 | Common:4; Rare:110 | ||||
chr20:23051595-23051601 | Rare:1 | ||||
chr20:23084421-23084651 | Common:1; Rare:81 | ||||
chr20:31604255-31604428 | Common:1; Rare:69 | ||||
chr20:31608576-31608792 | Rare:69 |