Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:93207121-93207284 | Common:2; Rare:76 | ||||
chr14:94081154-94081387 | Common:3; Rare:73 | ||||
chr14:96363388-96363550 | Common:1; Rare:53 | ||||
chr14:100376259-100376487 | Common:3; Rare:75 | ||||
chr14:102362858-102363097 | Rare:106 | ||||
chr14:103123359-103123461 | Rare:18 | ||||
chr14:103529016-103529226 | Common:1; Rare:60 | ||||
chr14:103562632-103562996 | Common:5; Rare:127; Clinvar (benign):1 | ||||
chr14:103629124-103629216 | Rare:46 | ||||
chr14:103715448-103715851 | Common:1; Rare:135 | ||||
chr14:105248476-105248608 | Common:4; Rare:68 | ||||
chr14:105419803-105419882 | Rare:14 | ||||
chr15:34101855-34102080 | Common:1; Rare:45 | ||||
chr15:35546153-35546227 | Rare:28 | ||||
chr15:40039106-40039308 | Rare:86 |