Proximal
stomach(Human) | 11870 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154352989-154353460 | Common:3; Rare:115; Clinvar:10; Clinvar (benign):11 | ||||
| chrX:154353552-154354047 | Common:5; Rare:97; Clinvar:5; Clinvar (benign):16 | ||||
| chrX:154354140-154354484 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):4 | ||||
| chrX:154359244-154359566 | Rare:73; Clinvar:8; Clinvar (benign):8 | ||||
| chrX:154359573-154359926 | Common:1; Rare:86; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chrX:154364195-154364734 | Common:2; Rare:121; Clinvar:8; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chrX:154365121-154365498 | Common:1; Rare:93; Clinvar:10; Clinvar (benign):13 | ||||
| chrX:154370573-154370727 | Rare:32 | ||||
| chrX:154374508-154374892 | Common:2; Rare:73 | ||||
| chrX:154398805-154398869 | Common:2; Rare:21 | ||||
| chrX:154409131-154409396 | Rare:46 | ||||
| chrX:154428462-154428707 | Common:2; Rare:43 | ||||
| chrX:154471292-154471501 | Rare:43 | ||||
| chrX:154486543-154486762 | Rare:30 | ||||
| chrX:154490614-154490858 | Common:2; Rare:56 |
- 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