Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:142438019-142438436 | Common:1; Rare:76 | ||||
chr3:142445802-142445835 | Rare:5 | ||||
chr3:142445933-142445995 | Rare:7 | ||||
chr3:142447419-142447477 | Common:1; Rare:22 | ||||
chr3:147410677-147411023 | Rare:84 | ||||
chr3:150408837-150408988 | Rare:46 | ||||
chr3:157174861-157175223 | Common:3; Rare:157 | ||||
chr3:164832208-164832350 | Rare:23 | ||||
chr3:169765038-169765268 | Rare:86; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr3:174330474-174330740 | Common:1; Rare:60 | ||||
chr3:174342076-174342497 | Rare:86 | ||||
chr3:183447427-183447674 | Common:2; Rare:63 | ||||
chr3:185175434-185175709 | Common:1; Rare:55 | ||||
chr3:193391926-193392262 | Common:3; Rare:57 | ||||
chr3:194071079-194071354 | Common:4; Rare:83 |