Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882159-179882318 | Common:1; Rare:31 | ||||
chr1:179882488-179882876 | Rare:189; Clinvar:8; Clinvar (benign):2 | ||||
chr1:180502348-180502640 | Common:1; Rare:100 | ||||
chr1:181482563-181482927 | Common:2; Rare:116 | ||||
chr1:182391334-182391494 | Rare:37 | ||||
chr1:182589195-182589317 | Rare:24 | ||||
chr1:182604383-182604541 | Rare:36 | ||||
chr1:182839280-182839435 | Rare:67 | ||||
chr1:183472281-183472522 | Common:2; Rare:84 | ||||
chr1:183635666-183636123 | Common:5; Rare:132 | ||||
chr1:185156701-185156826 | Common:1; Rare:47 | ||||
chr1:185156927-185157313 | Common:1; Rare:105 | ||||
chr1:185157439-185157527 | Common:1; Rare:32 | ||||
chr1:186375104-186375497 | Rare:112 | ||||
chr1:186375557-186375932 | Common:1; Rare:110 |