| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49585537-49585612 | Common:1; Rare:23 | ||||
| chr13:49936248-49936602 | Common:1; Rare:106 | ||||
| chr13:50081980-50082262 | Common:1; Rare:78 | ||||
| chr13:50910034-50910079 | Rare:12 | ||||
| chr13:51452542-51452577 | Rare:22 | ||||
| chr13:51453019-51453389 | Rare:143 | ||||
| chr13:51804084-51804249 | Common:2; Rare:49 | ||||
| chr13:52011905-52012421 | Common:2; Rare:170; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr13:52159558-52159634 | Common:1; Rare:17 | ||||
| chr13:52450576-52450689 | Rare:34 | ||||
| chr13:52455344-52455507 | Common:3; Rare:53 | ||||
| chr13:52652306-52652389 | Common:3; Rare:21 | ||||
| chr13:52652413-52652813 | Common:1; Rare:102 | ||||
| chr13:52652827-52652923 | Common:2; Rare:43 | ||||
| chr13:53028538-53029037 | Common:3; Rare:153 |