| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49792470-49792850 | Common:31; Rare:696 | ||||
| chr13:49792890-49793304 | Common:20; Rare:569 | ||||
| chr13:49935580-49936000 | Common:2; Rare:176 | ||||
| chr13:49936242-49936819 | Common:10; Rare:570 | ||||
| chr13:49996282-49996632 | Common:4; Rare:119 | ||||
| chr13:49996699-49997765 | Common:8; Rare:790 | ||||
| chr13:50081567-50081705 | Rare:30 | ||||
| chr13:50081825-50082344 | Common:7; Rare:660 | ||||
| chr13:50082658-50082854 | Common:1; Rare:47 | ||||
| chr13:50185918-50186609 | Common:15; Rare:252 | ||||
| chr13:50909546-50910619 | Common:15; Rare:699; Clinvar:14; Clinvar (benign):2 | ||||
| chr13:51451223-51452058 | Common:5; Rare:461 | ||||
| chr13:51451974-51452555 | Common:9; Rare:371 | ||||
| chr13:51452946-51454018 | Common:16; Rare:1510 | ||||
| chr13:51583747-51584597 | Common:17; Rare:685 |