Variant report

Variant	rs6948696
Chromosome Location	chr7:109172534-109172535
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10227434	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11765085	0.83[ASN][1000 genomes]
rs11771274	0.90[ASN][1000 genomes]
rs12154407	0.83[ASN][1000 genomes]
rs1524275	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1524276	1.00[ASN][1000 genomes]
rs1721904	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17461648	0.83[ASN][1000 genomes]
rs17461983	0.83[ASN][1000 genomes]
rs17462362	0.92[ASN][1000 genomes]
rs6950002	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6954194	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73713695	0.83[ASN][1000 genomes]
rs73713696	0.83[ASN][1000 genomes]
rs7778382	0.90[ASN][1000 genomes]
rs7780176	0.84[ASN][1000 genomes]
rs7787624	0.83[ASN][1000 genomes]
rs7802318	0.86[ASN][1000 genomes]
rs9886024	0.88[EUR][1000 genomes];0.90[ASN][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	nsv1023379	chr7:109003574-109355234	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv608079	chr7:109098364-109862289	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:109171800-109174200	Enhancers	Dnd41	blood
2	chr7:109172200-109173200	Enhancers	Fetal Intestine Small	intestine
3	chr7:109172400-109173000	Enhancers	Fetal Intestine Large	intestine

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