Proximal
stomach(Human) | 11870 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75982149-75982290 | Common:1; Rare:48; Clinvar:1 | ||||
| chr7:75983475-75983774 | Common:1; Rare:115; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr7:75992793-75992943 | Common:2; Rare:26 | ||||
| chr7:75994488-75994779 | Common:4; Rare:143 | ||||
| chr7:76047799-76048211 | Common:3; Rare:128 | ||||
| chr7:76302314-76302715 | Common:3; Rare:130; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:76302726-76303075 | Rare:152; Clinvar:14; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
| chr7:76303735-76303864 | Common:1; Rare:61; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:76303970-76303994 | Rare:11; Clinvar (benign):2 | ||||
| chr7:76397464-76397575 | Rare:51 | ||||
| chr7:76510439-76510596 | Rare:37 | ||||
| chr7:76625975-76626000 | Rare:8 | ||||
| chr7:76627251-76627363 | Common:5; Rare:30 | ||||
| chr7:77122036-77122672 | Common:4; Rare:133 | ||||
| chr7:77199521-77199751 | Common:2; Rare:58 |
- 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