Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:113208629-113208756 | Rare:73 | ||||
chr13:113209496-113209738 | Common:2; Rare:67 | ||||
chr13:113490673-113491120 | Common:4; Rare:171 | ||||
chr13:113863841-113864189 | Common:3; Rare:88 | ||||
chr13:114281505-114281657 | Common:2; Rare:82 | ||||
chr13:114281852-114282089 | Common:5; Rare:103 | ||||
chr14:20343219-20343644 | Common:12; Rare:242 | ||||
chr14:20454793-20455348 | Common:7; Rare:141 | ||||
chr14:20684438-20684630 | Common:2; Rare:32; Clinvar (benign):2 | ||||
chr14:20802796-20802970 | Common:1; Rare:23 | ||||
chr14:21022062-21022495 | Common:2; Rare:113 | ||||
chr14:21023548-21023682 | Common:1; Rare:15 | ||||
chr14:21024956-21025170 | Rare:79 | ||||
chr14:21025437-21026063 | Common:3; Rare:124 | ||||
chr14:21383938-21384098 | Common:6; Rare:61 |