| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49792498-49792706 | Common:5; Rare:93 | ||||
| chr13:49936234-49936601 | Common:1; Rare:110 | ||||
| chr13:49996722-49997092 | Common:1; Rare:80 | ||||
| chr13:50081943-50082312 | Common:1; Rare:105 | ||||
| chr13:50909691-50910079 | Common:1; Rare:83; Clinvar:5; Clinvar (benign):1 | ||||
| chr13:51453013-51453379 | Rare:140 | ||||
| chr13:51584208-51584522 | Common:3; Rare:106 | ||||
| chr13:51804103-51804244 | Common:2; Rare:44 | ||||
| chr13:52012084-52012428 | Common:2; Rare:111; Clinvar:1 | ||||
| chr13:52159553-52159662 | Common:1; Rare:21 | ||||
| chr13:52450579-52450698 | Rare:38 | ||||
| chr13:52455229-52455550 | Common:3; Rare:109 | ||||
| chr13:52455918-52456027 | Common:1; Rare:37 | ||||
| chr13:52652306-52652456 | Common:3; Rare:41 | ||||
| chr13:52652663-52652923 | Common:3; Rare:85 |