| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119165594-119165844 | Common:2; Rare:101; Clinvar:1; Clinvar (benign):5 | ||||
| chr10:119178458-119178583 | Common:1; Rare:33 | ||||
| chr10:119178634-119178705 | Common:1; Rare:12 | ||||
| chr10:119178711-119179083 | Common:3; Rare:122 | ||||
| chr10:119207148-119207195 | Rare:7 | ||||
| chr10:119207217-119207781 | Common:4; Rare:155 | ||||
| chr10:119542656-119542877 | Common:3; Rare:70 | ||||
| chr10:119543023-119543160 | Common:2; Rare:31 | ||||
| chr10:119595985-119596090 | Rare:20 | ||||
| chr10:119596384-119596465 | Rare:30 | ||||
| chr10:119596604-119596787 | Common:1; Rare:46 | ||||
| chr10:119596826-119597428 | Common:6; Rare:148 | ||||
| chr10:119650922-119651067 | Common:1; Rare:36 | ||||
| chr10:119651094-119651125 | Rare:8 | ||||
| chr10:119651156-119651580 | Common:7; Rare:143; Clinvar:1; Clinvar (benign):4 |