Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97445975-97446225 | Rare:66 | ||||
chr10:99430622-99430930 | Common:3; Rare:68 | ||||
chr10:99659264-99659529 | Common:1; Rare:66 | ||||
chr10:99732088-99732280 | Rare:60; Clinvar:3 | ||||
chr10:100185938-100186068 | Rare:53 | ||||
chr10:100987452-100987567 | Common:1; Rare:44; Clinvar (benign):1 | ||||
chr10:101588211-101588329 | Rare:48 | ||||
chr10:102714279-102714631 | Common:2; Rare:118 | ||||
chr10:103396419-103396699 | Rare:101 | ||||
chr10:110919348-110919629 | Common:7; Rare:77 | ||||
chr10:112446892-112447271 | Common:3; Rare:93 | ||||
chr10:119178790-119179003 | Common:3; Rare:71 | ||||
chr10:119892564-119892769 | Common:2; Rare:79 | ||||
chr10:122954208-122954486 | Rare:104 | ||||
chr10:123008791-123009006 | Common:5; Rare:58; Clinvar:3; Clinvar (benign):5 |