| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:98593581-98593847 | Common:3; Rare:169 | ||||
| chr3:98901617-98902070 | Common:2; Rare:309 | ||||
| chr3:99817543-99817972 | Rare:254 | ||||
| chr3:99818000-99818405 | Common:1; Rare:136 | ||||
| chr3:100260704-100261054 | Rare:192 | ||||
| chr3:100261110-100261440 | Common:1; Rare:127 | ||||
| chr3:100334633-100334847 | Common:3; Rare:157 | ||||
| chr3:100401004-100401247 | Rare:116 | ||||
| chr3:100401305-100401630 | Common:2; Rare:121 | ||||
| chr3:100492230-100492820 | Common:13; Rare:257 | ||||
| chr3:100709207-100709701 | Common:16; Rare:279; Clinvar (benign):2 | ||||
| chr3:101512540-101513010 | Common:6; Rare:184 | ||||
| chr3:101513108-101513375 | Common:16; Rare:109 | ||||
| chr3:101561744-101561980 | Common:4; Rare:145 | ||||
| chr3:101573600-101573910 | Common:1; Rare:133 |