Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:4094588-4094909 | Common:2; Rare:89 | ||||
chr11:4393671-4393814 | Rare:35 | ||||
chr11:4607810-4607981 | Common:3; Rare:52 | ||||
chr11:4608097-4608380 | Common:1; Rare:91 | ||||
chr11:5596440-5596810 | Common:11; Rare:115 | ||||
chr11:5624917-5625049 | Rare:21 | ||||
chr11:5685011-5685199 | Common:5; Rare:46 | ||||
chr11:6234606-6234937 | Common:2; Rare:93 | ||||
chr11:6390177-6390506 | Common:2; Rare:94 | ||||
chr11:6419037-6419233 | Common:3; Rare:46 | ||||
chr11:6473855-6474159 | Common:1; Rare:94 | ||||
chr11:6481295-6481566 | Common:5; Rare:127 | ||||
chr11:6603553-6603817 | Common:4; Rare:82; Clinvar (benign):3 | ||||
chr11:6604094-6605424 | Common:8; Rare:486; Clinvar (benign):10 | ||||
chr11:6607081-6607212 | Rare:41 |