Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:97764458-97764785 | Common:1; Rare:74; Clinvar (benign):1 | ||||
chr3:97821883-97822024 | Rare:46 | ||||
chr3:98901647-98902008 | Common:1; Rare:136 | ||||
chr3:99817579-99817938 | Rare:112 | ||||
chr3:100260715-100261015 | Rare:79 | ||||
chr3:100401398-100401582 | Common:1; Rare:34 | ||||
chr3:100709213-100709372 | Common:4; Rare:57 | ||||
chr3:101513122-101513319 | Common:8; Rare:41 | ||||
chr3:101561764-101561955 | Common:2; Rare:69 | ||||
chr3:101574042-101574230 | Rare:62 | ||||
chr3:101677098-101677175 | Rare:33 | ||||
chr3:105367153-105367273 | Common:1; Rare:28 | ||||
chr3:108090967-108091166 | Rare:75 | ||||
chr3:108222330-108222667 | Common:3; Rare:100 | ||||
chr3:108589422-108589699 | Common:3; Rare:67 |