Proximal
GM18507(Human) | 19257 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106629072-106629363 | Common:6; Rare:56 | ||||
| chr6:106629370-106629811 | Common:5; Rare:116 | ||||
| chr6:107028069-107028416 | Common:3; Rare:113 | ||||
| chr6:107028423-107028588 | Common:1; Rare:36 | ||||
| chr6:107114262-107114490 | Rare:70 | ||||
| chr6:107114675-107115035 | Common:3; Rare:102 | ||||
| chr6:107458994-107459143 | Rare:46; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:107459303-107459992 | Common:3; Rare:154; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:107957325-107957429 | Rare:19 | ||||
| chr6:107958027-107958464 | Common:2; Rare:143; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074344-108074347 | |||||
| chr6:108074644-108075000 | Common:2; Rare:121; Clinvar:1 | ||||
| chr6:108260183-108260491 | Common:2; Rare:78 | ||||
| chr6:108261130-108261498 | Common:2; Rare:130 | ||||
| chr6:108294702-108295254 | Common:2; Rare:177 |
- 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