| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49936241-49936569 | Common:1; Rare:99 | ||||
| chr13:49996715-49997099 | Common:1; Rare:89 | ||||
| chr13:50081969-50082267 | Common:1; Rare:83 | ||||
| chr13:50910028-50910074 | Rare:12 | ||||
| chr13:51804089-51804305 | Common:2; Rare:63 | ||||
| chr13:52012128-52012418 | Common:2; Rare:94; Clinvar:1 | ||||
| chr13:52406125-52406411 | Common:2; Rare:77 | ||||
| chr13:52455327-52455543 | Common:3; Rare:81 | ||||
| chr13:60163877-60164080 | Common:1; Rare:49 | ||||
| chr13:72727587-72727978 | Common:5; Rare:153 | ||||
| chr13:72781852-72782188 | Common:1; Rare:131 | ||||
| chr13:75549409-75549847 | Common:8; Rare:116 | ||||
| chr13:75636015-75636323 | Common:2; Rare:75 | ||||
| chr13:76991949-76992160 | Common:3; Rare:105; Clinvar:20; Clinvar (benign):12 | ||||
| chr13:79405785-79405870 | Rare:33 |