Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103562622-103563092 | Common:8; Rare:184; Clinvar (benign):5 | ||||
chr15:22838356-22838764 | Common:3; Rare:147 | ||||
chr15:23039545-23039687 | Common:1; Rare:59 | ||||
chr15:32615156-32615660 | Common:6; Rare:123 | ||||
chr15:34101821-34102083 | Common:1; Rare:59 | ||||
chr15:34588447-34588565 | Rare:35 | ||||
chr15:34988236-34988404 | Common:1; Rare:69 | ||||
chr15:35546141-35546231 | Rare:31 | ||||
chr15:39920096-39920356 | Common:1; Rare:44 | ||||
chr15:39933873-39934202 | Common:4; Rare:99 | ||||
chr15:40039091-40039349 | Rare:101 | ||||
chr15:40340307-40340326 | Rare:3 | ||||
chr15:40340907-40341104 | Common:3; Rare:56 | ||||
chr15:40565003-40565273 | Common:3; Rare:51 | ||||
chr15:40695081-40695227 | Common:2; Rare:44 |