Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:105706823-105706930 | Common:2; Rare:21 | ||||
chr13:106479129-106479268 | Rare:24 | ||||
chr13:107034755-107034906 | Rare:27 | ||||
chr13:107835491-107835615 | Rare:19 | ||||
chr13:108886059-108886121 | Common:2; Rare:19 | ||||
chr13:109454348-109454484 | Rare:24 | ||||
chr13:109892529-109892641 | Common:2; Rare:25 | ||||
chr13:110023583-110023709 | Rare:28 | ||||
chr13:110511813-110511977 | Common:3; Rare:46; Clinvar (benign):4 | ||||
chr13:110562454-110562463 | Rare:2 | ||||
chr13:110632418-110632479 | Common:1; Rare:21 | ||||
chr13:110870238-110870370 | Common:1; Rare:21 | ||||
chr13:111095675-111095879 | Common:3; Rare:26 | ||||
chr13:111588068-111588209 | Common:1; Rare:30 | ||||
chr13:111595811-111595973 | Rare:33 |