| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:36987946-36988233 | Common:1; Rare:55 | ||||
| chr3:37048434-37048574 | Rare:39; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr3:37067353-37067417 | Common:1; Rare:14 | ||||
| chr3:37074364-37074665 | Common:1; Rare:49 | ||||
| chr3:37074928-37075119 | Common:1; Rare:36 | ||||
| chr3:37142711-37142798 | Rare:13 | ||||
| chr3:37244150-37244418 | Common:2; Rare:79 | ||||
| chr3:37259527-37259710 | Common:2; Rare:23 | ||||
| chr3:37298833-37299316 | Rare:138 | ||||
| chr3:37963373-37963502 | Rare:25 | ||||
| chr3:38182795-38183068 | Rare:51 | ||||
| chr3:38184957-38185154 | Common:1; Rare:27 | ||||
| chr3:38235441-38235682 | Rare:36 | ||||
| chr3:38240728-38241023 | Common:2; Rare:62 | ||||
| chr3:38249733-38249984 | Common:1; Rare:40 |