| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:88165861-88166256 | Common:1; Rare:119 | ||||
| chr6:88963585-88963833 | Common:2; Rare:84 | ||||
| chr6:89352634-89353005 | Common:1; Rare:82 | ||||
| chr6:89638443-89638544 | Common:1; Rare:22 | ||||
| chr6:89638732-89638806 | Common:3; Rare:21 | ||||
| chr6:89819720-89819838 | Rare:41 | ||||
| chr6:89829614-89829964 | Rare:91 | ||||
| chr6:90296834-90297136 | Common:1; Rare:102 | ||||
| chr6:90587015-90587334 | Common:2; Rare:87 | ||||
| chr6:95577404-95577560 | Common:3; Rare:43 | ||||
| chr6:96521665-96521867 | Common:8; Rare:97 | ||||
| chr6:96522202-96522433 | Common:1; Rare:49 | ||||
| chr6:96897803-96898086 | Common:4; Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:96924335-96924702 | Common:4; Rare:95 | ||||
| chr6:97283143-97283437 | Common:3; Rare:83 |