| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156601411-156601612 | Common:2; Rare:65 | ||||
| chr1:156741071-156741395 | Common:1; Rare:89 | ||||
| chr1:157993514-157993666 | Common:1; Rare:45 | ||||
| chr1:158999706-159000028 | Common:2; Rare:70 | ||||
| chr1:160031965-160032060 | Rare:26 | ||||
| chr1:160098810-160099150 | Common:4; Rare:55 | ||||
| chr1:160205216-160205459 | Common:2; Rare:69 | ||||
| chr1:160343200-160343389 | Rare:76 | ||||
| chr1:160400410-160400786 | Common:2; Rare:90 | ||||
| chr1:161038903-161039049 | Common:1; Rare:51 | ||||
| chr1:161045888-161046057 | Common:1; Rare:44 | ||||
| chr1:161118022-161118137 | Rare:54 | ||||
| chr1:161132592-161132674 | Common:1; Rare:31 | ||||
| chr1:161159302-161159500 | Common:2; Rare:52 | ||||
| chr1:161166268-161166479 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):1 |