| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112379880-112380143 | Common:1; Rare:114 | ||||
| chr9:112718086-112718351 | Rare:58 | ||||
| chr9:113221262-113221594 | Rare:106 | ||||
| chr9:113275381-113275726 | Common:5; Rare:111; Clinvar (pathogenic):1 | ||||
| chr9:113410394-113410772 | Common:3; Rare:109 | ||||
| chr9:113565375-113565591 | Common:1; Rare:44 | ||||
| chr9:113593848-113594160 | Common:4; Rare:119 | ||||
| chr9:114587588-114587856 | Common:2; Rare:100 | ||||
| chr9:115118151-115118456 | Rare:70 | ||||
| chr9:116687235-116687364 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793257-120793528 | Common:1; Rare:98 | ||||
| chr9:120842905-120843113 | Common:1; Rare:74 | ||||
| chr9:120877162-120877516 | Common:2; Rare:124 | ||||
| chr9:121074849-121074967 | Rare:57 | ||||
| chr9:121201852-121202125 | Common:2; Rare:76 |