Variant report

Variant	rs7848519
Chromosome Location	chr9:99825018-99825019
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10759435	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1985682	1.00[ASN][1000 genomes]
rs4361859	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6477831	1.00[CHB][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes]
rs6477855	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6477872	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6477874	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7037968	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7848718	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7849720	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7862725	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7863880	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs7867279	1.00[CEU][hapmap];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428540	chr9:99722815-99863455	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv831662	chr9:99752521-99939231	Bivalent Enhancer Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99816200-99834600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:99823600-99825800	Enhancers	HMEC	breast
3	chr9:99823800-99825400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:99824200-99825400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:99824400-99825200	Enhancers	Stomach Mucosa	stomach
6	chr9:99824400-99825600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:99824400-99825600	Enhancers	Fetal Intestine Large	intestine
8	chr9:99824400-99825600	Enhancers	Fetal Intestine Small	intestine
9	chr9:99824600-99825400	Enhancers	NHEK	skin
10	chr9:99824600-99825600	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr9:99824800-99825200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr9:99824800-99825200	Enhancers	HepG2	liver
13	chr9:99825000-99825400	Enhancers	Hela-S3	cervix

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links