| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201118534-201118886 | Rare:52 | ||||
| chr2:201451389-201451826 | Common:2; Rare:114 | ||||
| chr2:201642653-201642764 | Rare:60 | ||||
| chr2:202376420-202376597 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:202912128-202912293 | Common:2; Rare:56 | ||||
| chr2:203014676-203014933 | Common:1; Rare:77 | ||||
| chr2:203238719-203239077 | Common:3; Rare:123 | ||||
| chr2:203239201-203239348 | Rare:49 | ||||
| chr2:203328187-203328430 | Common:2; Rare:92 | ||||
| chr2:203535250-203535546 | Common:3; Rare:129 | ||||
| chr2:206085772-206085960 | Common:1; Rare:54 | ||||
| chr2:206086280-206086384 | Rare:18 | ||||
| chr2:206159345-206159681 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr2:206159795-206160058 | Common:1; Rare:91 | ||||
| chr2:206274964-206275057 | Common:1; Rare:30 |