Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:132956269-132956370 | Common:1; Rare:26 | ||||
chr12:133130411-133130611 | Common:3; Rare:64 | ||||
chr13:19863478-19863964 | Common:6; Rare:177 | ||||
chr13:20773929-20774136 | Common:1; Rare:65 | ||||
chr13:23579189-23579451 | Common:6; Rare:89 | ||||
chr13:23889294-23889558 | Common:1; Rare:93 | ||||
chr13:27424543-27424746 | Common:2; Rare:66 | ||||
chr13:27450085-27450222 | Common:3; Rare:43 | ||||
chr13:30306991-30307204 | Common:5; Rare:51 | ||||
chr13:36297779-36297897 | Rare:42 | ||||
chr13:36346278-36346500 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
chr13:37000759-37000801 | Rare:22 | ||||
chr13:39038043-39038482 | Common:1; Rare:107 | ||||
chr13:40771145-40771446 | Common:3; Rare:84 | ||||
chr13:41060886-41061043 | Common:16; Rare:93 |