Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234356848-234357008 | Common:2; Rare:48 | ||||
chr1:234600059-234600289 | Common:7; Rare:99 | ||||
chr1:234610154-234610327 | Common:2; Rare:74 | ||||
chr1:236212714-236212950 | Rare:41 | ||||
chr1:244863715-244863833 | Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
chr10:4983982-4984069 | Rare:17 | ||||
chr10:5766518-5766813 | Common:2; Rare:60 | ||||
chr10:6163640-6163885 | Common:6; Rare:87 | ||||
chr10:23174526-23174709 | Rare:58 | ||||
chr10:23174833-23174989 | Common:4; Rare:48 | ||||
chr10:24118390-24118537 | Rare:36 | ||||
chr10:28302955-28303332 | Common:3; Rare:104 | ||||
chr10:29409453-29409615 | Common:2; Rare:50 | ||||
chr10:38356170-38356428 | Common:5; Rare:68 | ||||
chr10:42552786-42552994 | Common:1; Rare:64 |