Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:152984239-152984266 | Rare:2 | ||||
chr6:152984609-152984634 | Rare:4 | ||||
chr6:152992964-152993263 | Common:1; Rare:52 | ||||
chr6:158767059-158767450 | Common:4; Rare:163; Clinvar:2; Clinvar (benign):2 | ||||
chr6:158767454-158767787 | Common:3; Rare:105; Clinvar (benign):1 | ||||
chr6:158770866-158771067 | Common:1; Rare:44 | ||||
chr6:158815516-158815588 | Rare:10 | ||||
chr6:158867927-158868192 | Rare:46 | ||||
chr6:159690236-159690495 | Common:1; Rare:54 | ||||
chr6:159694296-159694326 | Rare:8 | ||||
chr6:159716329-159716473 | Rare:24 | ||||
chr6:159761304-159761442 | Common:1; Rare:26 | ||||
chr6:160992402-160992495 | Rare:28 | ||||
chr6:167850014-167850324 | Rare:45 | ||||
chr6:168367411-168367580 | Common:1; Rare:38 |