Proximal
A549(Human) | 8718 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34652007-34652220 | Rare:64 | ||||
| chr9:34665428-34665629 | Rare:62 | ||||
| chr9:35075278-35075555 | Rare:68; Clinvar:5; Clinvar (benign):2 | ||||
| chr9:35079883-35080157 | Common:5; Rare:71; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:35161786-35162141 | Common:4; Rare:102 | ||||
| chr9:35162283-35162347 | Rare:21 | ||||
| chr9:35489745-35490165 | Common:4; Rare:127 | ||||
| chr9:35605063-35605262 | Common:2; Rare:51 | ||||
| chr9:35646800-35646951 | Rare:35 | ||||
| chr9:35657990-35658365 | Common:6; Rare:274; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):33 | ||||
| chr9:35665155-35665376 | Common:2; Rare:80 | ||||
| chr9:35673713-35673951 | Common:2; Rare:49 | ||||
| chr9:35685434-35685783 | Common:1; Rare:80; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:35689704-35690097 | Common:3; Rare:126; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35698889-35699185 | Common:1; Rare:87 |
- 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