Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:96305449-96305654 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
chr2:96335717-96335790 | Common:1; Rare:22 | ||||
chr2:96868525-96868804 | Rare:70 | ||||
chr2:97645780-97646119 | Common:3; Rare:106 | ||||
chr2:98608420-98608649 | Common:1; Rare:102; Clinvar (benign):1 | ||||
chr2:99154857-99155041 | Common:2; Rare:80; Clinvar (benign):2 | ||||
chr2:99180971-99181240 | Common:2; Rare:77 | ||||
chr2:100562720-100563046 | Common:3; Rare:105 | ||||
chr2:102104385-102104688 | Common:6; Rare:70 | ||||
chr2:102141663-102141819 | Rare:27 | ||||
chr2:102736876-102736936 | Common:1; Rare:16 | ||||
chr2:105337479-105337606 | Common:1; Rare:59 | ||||
chr2:105396966-105397202 | Common:6; Rare:65 | ||||
chr2:105398978-105399245 | Common:1; Rare:96 | ||||
chr2:106194237-106194536 | Common:5; Rare:127 |