| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49496040-49496527 | Common:7; Rare:191 | ||||
| chr13:49585441-49585837 | Common:5; Rare:223 | ||||
| chr13:49585971-49586145 | Common:2; Rare:63 | ||||
| chr13:49628373-49628558 | Common:2; Rare:70 | ||||
| chr13:49691317-49691748 | Common:12; Rare:227 | ||||
| chr13:49792472-49792839 | Common:10; Rare:254 | ||||
| chr13:49792853-49793281 | Common:11; Rare:331 | ||||
| chr13:49935539-49935964 | Common:1; Rare:86 | ||||
| chr13:49936208-49936698 | Common:5; Rare:353 | ||||
| chr13:49996672-49997160 | Common:4; Rare:295 | ||||
| chr13:50081414-50081814 | Common:1; Rare:130 | ||||
| chr13:50081792-50082291 | Common:4; Rare:318 | ||||
| chr13:50185903-50186061 | Common:9; Rare:87 | ||||
| chr13:50185989-50186555 | Common:10; Rare:156 | ||||
| chr13:50909655-50910413 | Common:6; Rare:370; Clinvar:12; Clinvar (benign):2 |