| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136118727-136119044 | Common:5; Rare:119 | ||||
| chr9:136245810-136246080 | Common:3; Rare:57 | ||||
| chr9:136327313-136327611 | Common:4; Rare:112 | ||||
| chr9:136410423-136410738 | Common:7; Rare:142; Clinvar (pathogenic):1 | ||||
| chr9:136545839-136546291 | Common:2; Rare:162 | ||||
| chr9:136800121-136800399 | Common:5; Rare:86 | ||||
| chr9:136807780-136808174 | Common:3; Rare:150 | ||||
| chr9:136849287-136850136 | Common:4; Rare:337 | ||||
| chr9:136850656-136850860 | Common:1; Rare:88 | ||||
| chr9:136866193-136866469 | Common:3; Rare:99 | ||||
| chr9:136886249-136886537 | Common:2; Rare:84 | ||||
| chr9:136944592-136944919 | Common:2; Rare:128 | ||||
| chr9:137086613-137087136 | Common:2; Rare:219; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137111671-137111984 | Common:3; Rare:139 | ||||
| chr9:137112599-137112969 | Common:2; Rare:141 |