Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:106567955-106568267 | Rare:80 | ||||
chr13:108218307-108218520 | Rare:82 | ||||
chr13:110307155-110307421 | Common:4; Rare:88; Clinvar (benign):4 | ||||
chr13:110713008-110713261 | Common:2; Rare:111 | ||||
chr13:113208627-113208704 | Rare:48 | ||||
chr13:114281505-114281650 | Common:2; Rare:78 | ||||
chr14:20343212-20343635 | Common:12; Rare:247 | ||||
chr14:20413420-20413562 | Common:3; Rare:44 | ||||
chr14:20455062-20455287 | Common:2; Rare:70 | ||||
chr14:21437222-21437455 | Common:4; Rare:97 | ||||
chr14:21476925-21477275 | Common:1; Rare:102 | ||||
chr14:21511289-21511549 | Rare:66 | ||||
chr14:22766560-22766710 | Common:1; Rare:80 | ||||
chr14:22929363-22929609 | Rare:56 | ||||
chr14:23095093-23095594 | Common:3; Rare:221 |