Proximal
GM19238(Human) | 21581 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42542086-42542208 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:42842720-42842945 | Common:2; Rare:62 | ||||
| chr8:42842950-42843181 | Rare:75; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr8:42843189-42843626 | Common:3; Rare:118; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:42895951-42896246 | Common:1; Rare:85 | ||||
| chr8:42896253-42897115 | Common:3; Rare:367 | ||||
| chr8:42897266-42897447 | Common:1; Rare:50 | ||||
| chr8:43055730-43055785 | Common:1; Rare:5 | ||||
| chr8:43055969-43056479 | Common:2; Rare:156 | ||||
| chr8:43056482-43056774 | Common:1; Rare:85 | ||||
| chr8:43093375-43093547 | Common:2; Rare:34 | ||||
| chr8:43093826-43094048 | Common:1; Rare:50 | ||||
| chr8:43140233-43140290 | Rare:22 | ||||
| chr8:43140293-43140545 | Common:2; Rare:99; Clinvar:7 | ||||
| chr8:43140569-43140786 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):1 |
- Legend for epigenomic status:
- : Enriched for H3K27ac and DNaseI signal
- : Enriched for H3K4me3 and DNaseI signal
- : Enriched for CTCF binding signal
- Legend for core promoter element:
- : Found Initiator
- : Found DPR
- : Enriched TATA box