| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183659105-183659335 | Common:1; Rare:72 | ||||
| chr4:184649410-184649783 | Common:4; Rare:123 | ||||
| chr4:185396581-185396843 | Rare:83 | ||||
| chr4:185425866-185426272 | Common:4; Rare:124 | ||||
| chr4:189940613-189940991 | Common:11; Rare:134 | ||||
| chr5:218134-218361 | Common:3; Rare:90; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:612203-612357 | Rare:61 | ||||
| chr5:892533-892999 | Common:5; Rare:149 | ||||
| chr5:1799791-1799942 | Common:4; Rare:77 | ||||
| chr5:1801300-1801447 | Common:4; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378498-6378694 | Rare:79 | ||||
| chr5:6633005-6633386 | Common:8; Rare:120; Clinvar:9; Clinvar (benign):3 | ||||
| chr5:7869000-7869194 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr5:10249879-10250190 | Common:16; Rare:143 | ||||
| chr5:10250193-10250389 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):2 |