Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:106568082-106568267 | Rare:59 | ||||
chr13:108218313-108218520 | Rare:80 | ||||
chr13:110306959-110307526 | Common:7; Rare:176; Clinvar:3; Clinvar (benign):10 | ||||
chr13:110307619-110307920 | Common:3; Rare:88 | ||||
chr13:110561647-110561889 | Common:5; Rare:83 | ||||
chr13:111153614-111153721 | Common:2; Rare:47 | ||||
chr13:112689756-112690013 | Common:5; Rare:87 | ||||
chr13:113208614-113208775 | Rare:95 | ||||
chr13:113297049-113297262 | Common:1; Rare:84 | ||||
chr13:113364124-113364463 | Common:2; Rare:21 | ||||
chr13:113490683-113491258 | Common:4; Rare:206 | ||||
chr13:113759147-113759281 | Rare:38 | ||||
chr13:113863831-113864180 | Common:3; Rare:85 | ||||
chr13:114132482-114132729 | Rare:76 | ||||
chr13:114281519-114281654 | Common:2; Rare:75 |