Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:101445597-101445765 | Common:3; Rare:31 | ||||
chr15:101528335-101528478 | Common:1; Rare:31 | ||||
chr15:101613598-101613755 | Common:1; Rare:32 | ||||
chr15:101614267-101614478 | Common:1; Rare:38 | ||||
chr15:101961528-101961641 | Rare:4 | ||||
chr16:377141-377462 | Common:5; Rare:145 | ||||
chr16:405836-406097 | Common:3; Rare:58 | ||||
chr16:1361937-1362091 | Common:1; Rare:81; Clinvar:1; Clinvar (pathogenic):5 | ||||
chr16:1362112-1362260 | Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2171335-2171593 | Common:1; Rare:90 | ||||
chr16:2673378-2673691 | Common:8; Rare:109 | ||||
chr16:3020929-3021293 | Rare:111 | ||||
chr16:3143841-3143980 | Rare:32 | ||||
chr16:3695939-3696146 | Rare:60 | ||||
chr16:4307570-4307839 | Common:3; Rare:97 |