Proximal
A549(Human) | 8718 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:24055218-24055325 | Rare:18 | ||||
| chrX:24148842-24149001 | Common:1; Rare:27 | ||||
| chrX:24693770-24694000 | Common:2; Rare:43 | ||||
| chrX:30308169-30308986 | Common:1; Rare:176; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chrX:30309092-30309245 | Rare:41 | ||||
| chrX:30309308-30309514 | Rare:50; Clinvar (benign):1 | ||||
| chrX:40735532-40735640 | Rare:32 | ||||
| chrX:41333752-41333955 | Common:2; Rare:54 | ||||
| chrX:44872910-44873188 | Rare:47 | ||||
| chrX:46545374-46545570 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chrX:46912241-46912714 | Rare:110 | ||||
| chrX:47144654-47144843 | Common:1; Rare:31 | ||||
| chrX:47145051-47145480 | Common:2; Rare:72 | ||||
| chrX:47193785-47193967 | Common:1; Rare:33; Clinvar:1 | ||||
| chrX:47202145-47202502 | Rare:82; Clinvar:3; Clinvar (benign):5 |
- 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