| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123973413-123973490 | Common:2; Rare:16 | ||||
| chr12:128823956-128824111 | Common:1; Rare:53 | ||||
| chr12:132144309-132144489 | Rare:73 | ||||
| chr12:132687334-132687662 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:132710748-132710878 | Common:3; Rare:56 | ||||
| chr12:132761797-132762154 | Common:3; Rare:124 | ||||
| chr12:132956244-132956417 | Common:1; Rare:40 | ||||
| chr12:133130260-133130652 | Common:7; Rare:130 | ||||
| chr13:19633463-19633854 | Common:3; Rare:147 | ||||
| chr13:19633925-19633961 | Rare:16 | ||||
| chr13:19782923-19783088 | Common:2; Rare:59 | ||||
| chr13:19863506-19863947 | Common:6; Rare:167 | ||||
| chr13:19958439-19958879 | Common:7; Rare:196 | ||||
| chr13:20703030-20703175 | Common:1; Rare:24 | ||||
| chr13:21140390-21140636 | Rare:112 |