| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51453013-51453308 | Rare:102 | ||||
| chr13:51804113-51804219 | Common:2; Rare:36 | ||||
| chr13:52455327-52455517 | Common:3; Rare:65 | ||||
| chr13:52652666-52652916 | Common:3; Rare:80 | ||||
| chr13:60163886-60164095 | Common:1; Rare:52 | ||||
| chr13:72727591-72727972 | Common:4; Rare:147 | ||||
| chr13:72781853-72782188 | Common:1; Rare:130 | ||||
| chr13:75549440-75549823 | Common:8; Rare:99 | ||||
| chr13:76991905-76992175 | Common:3; Rare:119; Clinvar:20; Clinvar (benign):15 | ||||
| chr13:93227096-93227431 | Common:1; Rare:77; Clinvar:5; Clinvar (benign):1 | ||||
| chr13:95676926-95677187 | Common:3; Rare:91 | ||||
| chr13:96053378-96053477 | Common:1; Rare:36 | ||||
| chr13:99200668-99200896 | Common:6; Rare:105 | ||||
| chr13:100088844-100089117 | Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:102596801-102597028 | Common:1; Rare:106 |