| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:47959975-47960025 | Rare:15; Clinvar (benign):1 | ||||
| chr8:47960034-47960267 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:47960668-47961004 | Common:2; Rare:130; Clinvar:11; Clinvar (benign):1 | ||||
| chr8:48008348-48008464 | Common:2; Rare:70 | ||||
| chr8:51898972-51899340 | Common:8; Rare:162 | ||||
| chr8:52714356-52714587 | Common:1; Rare:102 | ||||
| chr8:53843200-53843328 | Common:1; Rare:32 | ||||
| chr8:54021921-54022035 | Rare:51 | ||||
| chr8:54022063-54022182 | Rare:47 | ||||
| chr8:54022261-54022513 | Common:1; Rare:81 | ||||
| chr8:54101755-54102202 | Common:3; Rare:173 | ||||
| chr8:54135154-54135308 | Common:2; Rare:49 | ||||
| chr8:55773288-55773669 | Common:4; Rare:132 | ||||
| chr8:56074065-56074266 | Common:8; Rare:90 | ||||
| chr8:56074384-56074724 | Common:6; Rare:138 |