| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136289767-136290054 | Common:2; Rare:124 | ||||
| chr6:136550371-136550695 | Common:2; Rare:99 | ||||
| chr6:136791722-136792246 | Common:3; Rare:134 | ||||
| chr6:136792536-136792626 | Rare:34 | ||||
| chr6:136792857-136793247 | Common:1; Rare:98 | ||||
| chr6:137044115-137044218 | Common:2; Rare:23 | ||||
| chr6:137044661-137044755 | Rare:24 | ||||
| chr6:137219111-137219209 | Common:1; Rare:28 | ||||
| chr6:137219262-137219527 | Common:4; Rare:93; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:137867042-137867315 | Rare:63 | ||||
| chr6:138404178-138404595 | Common:7; Rare:118 | ||||
| chr6:138773442-138773597 | Common:2; Rare:93 | ||||
| chr6:138773657-138773876 | Common:3; Rare:98 | ||||
| chr6:139374411-139374667 | Common:3; Rare:116 | ||||
| chr6:142147140-142147290 | Rare:56 |