| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51803413-51803585 | Common:1; Rare:29 | ||||
| chr13:51803669-51803909 | Rare:68 | ||||
| chr13:51803924-51804032 | Rare:29 | ||||
| chr13:51804092-51804381 | Common:2; Rare:77 | ||||
| chr13:52012115-52012489 | Common:2; Rare:143; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:52158876-52159079 | Common:3; Rare:46 | ||||
| chr13:52450010-52450367 | Common:2; Rare:76 | ||||
| chr13:52450541-52450852 | Common:1; Rare:87 | ||||
| chr13:52454604-52454934 | Common:1; Rare:60 | ||||
| chr13:52455076-52455176 | Common:2; Rare:20 | ||||
| chr13:52455180-52455594 | Common:4; Rare:136 | ||||
| chr13:52455836-52456022 | Common:4; Rare:57 | ||||
| chr13:52652027-52652482 | Common:3; Rare:117 | ||||
| chr13:52652509-52653014 | Common:3; Rare:155 | ||||
| chr13:52653098-52653230 | Common:1; Rare:41 |