Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:100731210-100732100 | Common:4; Rare:252 | ||||
| chrX:100820118-100820869 | Common:18; Rare:391 | ||||
| chrX:101051250-101051755 | Common:3; Rare:148 | ||||
| chrX:101051760-101052340 | Common:5; Rare:260 | ||||
| chrX:101097852-101098287 | Common:7; Rare:321 | ||||
| chrX:101348026-101348642 | Common:3; Rare:120; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chrX:101348558-101349242 | Common:23; Rare:377; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chrX:101385381-101386435 | Common:6; Rare:264; Clinvar:1 | ||||
| chrX:101386345-101387183 | Common:4; Rare:130 | ||||
| chrX:101390061-101390772 | Common:3; Rare:128; Clinvar (benign):1 | ||||
| chrX:101390711-101391540 | Common:6; Rare:585 | ||||
| chrX:101407536-101407697 | Common:1; Rare:17; Clinvar (benign):1 | ||||
| chrX:101407787-101408298 | Common:30; Rare:471; Clinvar:9; Clinvar (benign):64 | ||||
| chrX:101408275-101408499 | Rare:45 | ||||
| chrX:101408684-101409345 | Common:8; Rare:132 |
- 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