| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24793102-24793161 | Rare:32 | ||||
| chr2:24971900-24972145 | Common:1; Rare:80 | ||||
| chr2:25878275-25878409 | Rare:31 | ||||
| chr2:26033792-26034146 | Common:3; Rare:125 | ||||
| chr2:26034339-26034732 | Common:2; Rare:93 | ||||
| chr2:26194568-26194791 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26244557-26244754 | Rare:76; Clinvar:2; Clinvar (benign):5 | ||||
| chr2:26244762-26244988 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:26345798-26346165 | Common:1; Rare:110 | ||||
| chr2:26764185-26764409 | Common:3; Rare:77 | ||||
| chr2:27032862-27033004 | Rare:55 | ||||
| chr2:27071545-27071888 | Common:1; Rare:103 | ||||
| chr2:27086601-27086759 | Rare:46 | ||||
| chr2:27211794-27212115 | Common:3; Rare:107 | ||||
| chr2:27212242-27212437 | Common:2; Rare:103 |