Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:101915106-101915228 | Rare:23 | ||||
chr11:102317234-102317546 | Rare:60 | ||||
chr11:102347111-102347323 | Common:2; Rare:71 | ||||
chr11:102452546-102452944 | Common:2; Rare:129 | ||||
chr11:102797987-102798246 | Common:1; Rare:79 | ||||
chr11:103092034-103092259 | Common:1; Rare:68 | ||||
chr11:106077326-106077711 | Common:2; Rare:115 | ||||
chr11:108009273-108009349 | Rare:38 | ||||
chr11:108121434-108121634 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):5 | ||||
chr11:108222580-108222954 | Rare:124; Clinvar:3 | ||||
chr11:110296515-110296784 | Rare:130; Clinvar:7 | ||||
chr11:111766348-111766426 | Rare:40 | ||||
chr11:111871302-111871582 | Common:3; Rare:100; Clinvar:4; Clinvar (benign):2 | ||||
chr11:111879158-111879541 | Rare:113 | ||||
chr11:112073995-112074357 | Common:1; Rare:75 |