Variant report

Variant	rs10486783
Chromosome Location	chr7:15944974-15944975
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10486786	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10950594	1.00[AMR][1000 genomes]
rs11980623	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11984407	0.87[AMR][1000 genomes]
rs12666423	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12669371	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12674322	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1406100	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17169154	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4382357	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58428788	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60024014	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60774259	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61121193	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv523199	chr7:15582208-16042596	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv1017958	chr7:15910153-15956470	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 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	chr7:15944800-15945000	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr7:15944800-15946400	Enhancers	Rectal Smooth Muscle	rectum
3	chr7:15944800-15946800	Enhancers	Colon Smooth Muscle	Colon

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