Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103529070-103529233 | Common:1; Rare:50 | ||||
chr14:103562224-103562375 | Rare:62 | ||||
chr14:103562623-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
chr14:103629111-103629409 | Common:2; Rare:119 | ||||
chr14:103684352-103684526 | Rare:28 | ||||
chr14:103691933-103692195 | Rare:45 | ||||
chr14:103715470-103715883 | Common:1; Rare:131 | ||||
chr14:104775140-104775434 | Common:3; Rare:79; Clinvar:2; Clinvar (benign):3 | ||||
chr14:104924602-104924894 | Common:2; Rare:65 | ||||
chr14:104970465-104970567 | Common:2; Rare:20 | ||||
chr14:105021070-105021387 | Common:1; Rare:113 | ||||
chr14:105419751-105420018 | Rare:81 | ||||
chr15:22980292-22980476 | Rare:66 | ||||
chr15:25438984-25439209 | Common:2; Rare:84 | ||||
chr15:29821701-29821947 | Common:1; Rare:115 |