Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:35476296-35476759 | Common:1; Rare:82 | ||||
chr13:36131364-36131486 | Rare:34 | ||||
chr13:36297787-36297904 | Rare:41 | ||||
chr13:36345535-36345657 | Common:1; Rare:24 | ||||
chr13:36346073-36346459 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
chr13:36346582-36346841 | Common:4; Rare:72 | ||||
chr13:36920124-36920437 | Common:8; Rare:135; Clinvar:6; Clinvar (benign):2 | ||||
chr13:36999236-36999451 | Rare:94 | ||||
chr13:37000259-37000407 | Common:2; Rare:27 | ||||
chr13:37000518-37000815 | Common:3; Rare:96; Clinvar (pathogenic):1 | ||||
chr13:37059448-37059731 | Common:1; Rare:82 | ||||
chr13:37598615-37598678 | Rare:30 | ||||
chr13:38349793-38349920 | Common:1; Rare:65 | ||||
chr13:38350208-38350408 | Rare:66 | ||||
chr13:38686783-38687143 | Common:4; Rare:105; Clinvar:3; Clinvar (benign):1 |