| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49132897-49133141 | Rare:49; Clinvar:2 | ||||
| chr3:49166289-49166394 | Common:1; Rare:29 | ||||
| chr3:49171448-49171647 | Common:2; Rare:40 | ||||
| chr3:49191815-49191957 | Rare:23 | ||||
| chr3:49199096-49199783 | Common:2; Rare:148 | ||||
| chr3:49276981-49277132 | Common:1; Rare:53 | ||||
| chr3:49340003-49340125 | Common:2; Rare:57 | ||||
| chr3:49358267-49358434 | Common:2; Rare:96 | ||||
| chr3:49411820-49412432 | Common:2; Rare:213 | ||||
| chr3:49429238-49429508 | Common:1; Rare:68 | ||||
| chr3:49470004-49470325 | Common:1; Rare:96 | ||||
| chr3:49674212-49674556 | Common:1; Rare:125 | ||||
| chr3:49689451-49689616 | Rare:55 | ||||
| chr3:49723893-49724208 | Common:9; Rare:105 | ||||
| chr3:49786404-49786785 | Rare:111 |