Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110007805-110008106 | Common:1; Rare:74 | ||||
chr10:110304870-110305049 | Common:2; Rare:65 | ||||
chr10:110567426-110567804 | Common:2; Rare:111; Clinvar:2; Clinvar (benign):5 | ||||
chr10:110871655-110871964 | Rare:99 | ||||
chr10:110918923-110918953 | Rare:8 | ||||
chr10:110919134-110919636 | Common:8; Rare:133 | ||||
chr10:111076906-111077039 | Rare:34 | ||||
chr10:112183708-112183860 | Common:3; Rare:58 | ||||
chr10:112446723-112447284 | Common:3; Rare:134 | ||||
chr10:113854177-113854649 | Rare:95 | ||||
chr10:113854811-113854874 | Rare:21 | ||||
chr10:114174147-114174296 | Rare:61 | ||||
chr10:114821647-114821985 | Common:1; Rare:110 | ||||
chr10:116849416-116849564 | Common:1; Rare:43 | ||||
chr10:116849711-116849830 | Rare:42 |