Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:103093170-103093433 | Rare:55 | ||||
chr10:103661075-103661372 | Common:1; Rare:78 | ||||
chr10:103668729-103668858 | Rare:36 | ||||
chr10:104034112-104034495 | Rare:151; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr10:104045756-104045846 | Rare:38; Clinvar:1 | ||||
chr10:104322383-104322694 | Rare:54 | ||||
chr10:104326420-104326431 | Rare:2 | ||||
chr10:104335573-104335592 | Rare:2 | ||||
chr10:110211171-110211375 | Common:1; Rare:50 | ||||
chr10:110500793-110501030 | Common:1; Rare:46 | ||||
chr10:114515480-114515837 | Common:1; Rare:55 | ||||
chr10:114517064-114517236 | Common:1; Rare:25 | ||||
chr10:114538452-114538741 | Common:2; Rare:54 | ||||
chr10:114545170-114545286 | Common:3; Rare:18 | ||||
chr10:122063278-122063534 | Common:5; Rare:54 |