| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:135851560-135851786 | Rare:40 | ||||
| chr6:136250265-136250568 | Common:2; Rare:92 | ||||
| chr6:136289129-136289472 | Rare:121 | ||||
| chr6:136289761-136290063 | Common:2; Rare:134 | ||||
| chr6:136525727-136525917 | Rare:33 | ||||
| chr6:136525930-136526682 | Common:9; Rare:153 | ||||
| chr6:136550348-136550687 | Common:2; Rare:103 | ||||
| chr6:136792515-136792679 | Common:2; Rare:50 | ||||
| chr6:136793017-136793111 | Rare:23 | ||||
| chr6:137219310-137219493 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:137866972-137867285 | Rare:74 | ||||
| chr6:137870808-137871161 | Common:2; Rare:69 | ||||
| chr6:138107127-138107237 | Rare:35 | ||||
| chr6:138404161-138404560 | Common:7; Rare:110 | ||||
| chr6:138545667-138545860 | Common:1; Rare:36 |