Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:140049185-140049507 | Rare:50 | ||||
chr4:140096106-140096408 | Rare:51 | ||||
chr4:140118098-140118143 | Common:1; Rare:7 | ||||
chr4:145110104-145110444 | Rare:76 | ||||
chr4:147636666-147636975 | Common:3; Rare:57 | ||||
chr4:147637277-147637486 | Rare:39 | ||||
chr4:147637639-147637740 | Common:1; Rare:16 | ||||
chr4:151104644-151104788 | Rare:32 | ||||
chr4:151234513-151234729 | Common:4; Rare:27 | ||||
chr4:158715324-158715682 | Common:2; Rare:99 | ||||
chr4:160026868-160026949 | Rare:17 | ||||
chr4:163064024-163064290 | Common:2; Rare:31 | ||||
chr4:163093950-163094078 | Common:1; Rare:25 | ||||
chr4:168487651-168487913 | Common:3; Rare:31 | ||||
chr4:168925993-168926330 | Rare:61; Clinvar:3; Clinvar (benign):2 |