Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101694425-101694693 | Common:4; Rare:86; Clinvar:3; Clinvar (benign):5 | ||||
chr10:102121392-102121609 | Rare:34 | ||||
chr10:102643187-102643420 | Common:3; Rare:50 | ||||
chr10:102777073-102777315 | Common:2; Rare:41 | ||||
chr10:103192445-103192652 | Rare:50 | ||||
chr10:103668729-103668841 | Rare:34 | ||||
chr10:110211144-110211415 | Common:1; Rare:64 | ||||
chr10:110895806-110896078 | Rare:71 | ||||
chr10:112951485-112951748 | Common:2; Rare:92 | ||||
chr10:114632019-114632190 | Rare:47 | ||||
chr10:114822915-114822975 | Rare:7 | ||||
chr10:122113713-122113796 | Rare:25 | ||||
chr10:124010904-124010999 | Rare:29 | ||||
chr10:124916692-124916920 | Common:2; Rare:80 | ||||
chr10:124983174-124983504 | Common:1; Rare:69 |