| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203535126-203535546 | Common:3; Rare:155 | ||||
| chr2:203535779-203535845 | Rare:15 | ||||
| chr2:205682351-205682583 | Rare:41 | ||||
| chr2:205682837-205683136 | Common:1; Rare:39 | ||||
| chr2:206085435-206085718 | Common:4; Rare:76 | ||||
| chr2:206085765-206085983 | Common:1; Rare:63 | ||||
| chr2:206086007-206086121 | Common:1; Rare:25 | ||||
| chr2:206086127-206086275 | Rare:16 | ||||
| chr2:206086280-206086305 | Rare:3 | ||||
| chr2:206159345-206159549 | Common:3; Rare:57; Clinvar (benign):1 | ||||
| chr2:206159552-206160058 | Common:1; Rare:157 | ||||
| chr2:206274909-206275067 | Common:1; Rare:56 | ||||
| chr2:206765267-206765659 | Common:3; Rare:112; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166142 | Rare:42 | ||||
| chr2:207166182-207166387 | Common:3; Rare:90 |