Proximal
A549(Human) | 8718 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:75156235-75156382 | Common:2; Rare:43 | ||||
| chrX:75274640-75274733 | Common:1; Rare:16 | ||||
| chrX:76172727-76173202 | Rare:93 | ||||
| chrX:77522354-77522414 | Rare:8; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:77633246-77633676 | Rare:61; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chrX:77652267-77652461 | Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chrX:77652514-77652769 | Rare:23 | ||||
| chrX:77895396-77895753 | Rare:102; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78104167-78104394 | Common:3; Rare:93 | ||||
| chrX:78122804-78123279 | Rare:83; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chrX:78125021-78125332 | Rare:55; Clinvar:1 | ||||
| chrX:80809863-80810176 | Rare:40 | ||||
| chrX:81201873-81202166 | Rare:46 | ||||
| chrX:100820282-100820451 | Common:2; Rare:39 | ||||
| chrX:101051849-101052237 | Common:2; Rare:64 |
- 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