Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:29850330-29850429 | Common:1; Rare:28 | ||||
chr13:30306820-30307197 | Common:7; Rare:100 | ||||
chr13:30307374-30307745 | Common:5; Rare:111 | ||||
chr13:30465757-30466134 | Common:1; Rare:116 | ||||
chr13:30617284-30618052 | Common:1; Rare:235 | ||||
chr13:30735407-30735612 | Common:2; Rare:48 | ||||
chr13:31161666-31161726 | Rare:30 | ||||
chr13:32538640-32538973 | Common:1; Rare:89 | ||||
chr13:32586219-32586582 | Common:2; Rare:108 | ||||
chr13:33206021-33206123 | Rare:23 | ||||
chr13:33285687-33285864 | Rare:35 | ||||
chr13:36346249-36346488 | Common:3; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
chr13:36999254-36999459 | Rare:84 | ||||
chr13:37000243-37000391 | Common:2; Rare:26 | ||||
chr13:37000662-37000808 | Rare:59 |