Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:185821122-185821327 | Rare:37 | ||||
chr3:186567293-186567403 | Common:3; Rare:29 | ||||
chr3:186783226-186783598 | Common:2; Rare:145 | ||||
chr3:186806411-186806575 | Rare:58 | ||||
chr3:193593095-193593372 | Rare:91; Clinvar:2; Clinvar (benign):2 | ||||
chr3:196318184-196318324 | Common:1; Rare:63 | ||||
chr3:196432385-196432550 | Common:1; Rare:73 | ||||
chr3:197749777-197749968 | Common:1; Rare:75 | ||||
chr3:197791074-197791290 | Common:3; Rare:75 | ||||
chr3:197949894-197950298 | Common:4; Rare:121; Clinvar (benign):2 | ||||
chr4:474116-474343 | Common:2; Rare:76 | ||||
chr4:499136-499297 | Common:3; Rare:60 | ||||
chr4:674253-674553 | Common:1; Rare:138 | ||||
chr4:932259-932476 | Common:2; Rare:83 | ||||
chr4:1289663-1289911 | Common:1; Rare:79 |