| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:92298977-92299070 | Common:1; Rare:45; Clinvar:1 | ||||
| chr1:92484575-92484783 | Common:1; Rare:42 | ||||
| chr1:92831891-92832113 | Common:1; Rare:103; Clinvar:6; Clinvar (benign):5 | ||||
| chr1:93079064-93079290 | Common:3; Rare:99 | ||||
| chr1:93180337-93180736 | Common:1; Rare:168 | ||||
| chr1:93345773-93345946 | Common:4; Rare:67 | ||||
| chr1:93879144-93879338 | Common:3; Rare:73 | ||||
| chr1:94418216-94418455 | Common:2; Rare:79 | ||||
| chr1:95072866-95073018 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr1:96721589-96721840 | Common:2; Rare:117 | ||||
| chr1:99766620-99766749 | Rare:25 | ||||
| chr1:99850005-99850136 | Common:1; Rare:51 | ||||
| chr1:99969912-99970062 | Rare:38 | ||||
| chr1:100037973-100038143 | Common:1; Rare:69 | ||||
| chr1:100132891-100133237 | Common:2; Rare:134 |