Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:226984957-226985340 | Common:2; Rare:139; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:227542355-227542423 | Rare:9 | ||||
chr1:227945871-227946206 | Common:3; Rare:52 | ||||
chr1:228096786-228097262 | Rare:94 | ||||
chr1:228736335-228736474 | Rare:28 | ||||
chr1:229328712-229328940 | Common:3; Rare:28 | ||||
chr1:229330160-229330225 | Common:1; Rare:6 | ||||
chr1:229563747-229564022 | Common:2; Rare:37 | ||||
chr1:230770520-230770552 | Rare:8 | ||||
chr1:230799735-230800031 | Common:2; Rare:46 | ||||
chr1:230804136-230804433 | Common:3; Rare:58 | ||||
chr1:230999857-231000196 | Common:1; Rare:54 | ||||
chr1:231267871-231268156 | Common:2; Rare:53 | ||||
chr1:231363137-231363259 | Rare:22 | ||||
chr1:233707508-233707808 | Common:2; Rare:55 |