Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:139561727-139561800 | Rare:31 | ||||
chr5:140043240-140043331 | Rare:24 | ||||
chr5:140107730-140107797 | Rare:14 | ||||
chr5:140175017-140175241 | Rare:60 | ||||
chr5:140303030-140303171 | Common:1; Rare:46 | ||||
chr5:140401393-140401912 | Common:3; Rare:119 | ||||
chr5:140557372-140557555 | Common:3; Rare:118 | ||||
chr5:140564267-140564357 | Common:1; Rare:27 | ||||
chr5:140564475-140564935 | Rare:110 | ||||
chr5:140647382-140648131 | Common:19; Rare:304; Clinvar:4; Clinvar (benign):5 | ||||
chr5:140664717-140664915 | Common:3; Rare:53 | ||||
chr5:140691282-140691655 | Common:2; Rare:137; Clinvar:12; Clinvar (benign):2 | ||||
chr5:140794793-140794877 | Rare:18 | ||||
chr5:140807001-140807091 | Common:1; Rare:13 | ||||
chr5:140856432-140856532 | Rare:31 |