| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2047242-2047460 | Rare:52 | ||||
| chr16:2047784-2048058 | Rare:135; Clinvar:2; Clinvar (benign):5 | ||||
| chr16:2205695-2205917 | Common:4; Rare:103 | ||||
| chr16:2223304-2223688 | Rare:155 | ||||
| chr16:2268053-2268580 | Common:5; Rare:188 | ||||
| chr16:2340606-2341065 | Common:4; Rare:155; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:2429155-2429472 | Common:2; Rare:100 | ||||
| chr16:2459954-2460127 | Rare:44 | ||||
| chr16:2474966-2475160 | Rare:61; Clinvar (benign):2 | ||||
| chr16:2513645-2514014 | Rare:128 | ||||
| chr16:2537697-2538131 | Common:4; Rare:163 | ||||
| chr16:2682359-2682628 | Rare:125 | ||||
| chr16:2752245-2752464 | Common:1; Rare:65 | ||||
| chr16:2752535-2752671 | Rare:47 | ||||
| chr16:2770341-2770665 | Common:2; Rare:158 |