| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30466133-30467129 | Common:8; Rare:245 | ||||
| chr13:30616829-30618044 | Common:7; Rare:1492 | ||||
| chr13:30618166-30618784 | Common:7; Rare:176 | ||||
| chr13:31161345-31161745 | Common:3; Rare:196 | ||||
| chr13:31161822-31162607 | Common:16; Rare:1205 | ||||
| chr13:31199570-31200176 | Common:3; Rare:377; Clinvar:2 | ||||
| chr13:31200080-31200420 | Common:2; Rare:103; Clinvar:2 | ||||
| chr13:32261500-32261930 | Rare:108 | ||||
| chr13:32315220-32315700 | Common:7; Rare:373; Clinvar:14; Clinvar (benign):17 | ||||
| chr13:32315832-32316248 | Common:7; Rare:200; Clinvar (benign):10 | ||||
| chr13:32537770-32538578 | Common:4; Rare:236 | ||||
| chr13:32538589-32539271 | Common:8; Rare:770 | ||||
| chr13:32586105-32586626 | Common:12; Rare:721 | ||||
| chr13:32586942-32587238 | Common:6; Rare:170 | ||||
| chr13:33817830-33818360 | Common:10; Rare:692 |