| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237627371-237627668 | Common:2; Rare:101 | ||||
| chr2:238060744-238061075 | Common:5; Rare:102 | ||||
| chr2:238203565-238203810 | Common:5; Rare:97 | ||||
| chr2:239401641-239401730 | Rare:39 | ||||
| chr2:240025275-240025490 | Common:3; Rare:85; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240560756-240560882 | Common:1; Rare:57 | ||||
| chr2:240998239-240998376 | Rare:28 | ||||
| chr2:241040226-241040358 | Rare:30 | ||||
| chr2:241048075-241048421 | Common:1; Rare:75 | ||||
| chr2:241051017-241051309 | Common:2; Rare:56 | ||||
| chr2:241096354-241096626 | Rare:58 | ||||
| chr2:241102276-241102517 | Common:2; Rare:70 | ||||
| chr2:241236735-241237024 | Common:7; Rare:82 | ||||
| chr2:241272794-241272990 | Rare:73 | ||||
| chr2:241315109-241315401 | Common:5; Rare:98 |