Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102246119-102246341 | Common:2; Rare:35 | ||||
chr14:102305054-102305319 | Common:1; Rare:79 | ||||
chr14:102316901-102317215 | Common:7; Rare:175 | ||||
chr14:102362852-102363112 | Rare:113 | ||||
chr14:103333945-103334252 | Common:2; Rare:125 | ||||
chr14:103335915-103336118 | Rare:79 | ||||
chr14:103529035-103529243 | Common:1; Rare:64 | ||||
chr14:103562623-103563263 | Common:11; Rare:262; Clinvar:1; Clinvar (benign):9 | ||||
chr14:103715437-103715841 | Common:1; Rare:131 | ||||
chr14:104970471-104970573 | Common:3; Rare:18 | ||||
chr14:104985628-104985810 | Common:3; Rare:71 | ||||
chr14:105021014-105021421 | Common:1; Rare:148 | ||||
chr14:105398243-105398555 | Common:5; Rare:97 | ||||
chr14:105419742-105420038 | Rare:93 | ||||
chr15:22838356-22838710 | Common:3; Rare:127 |