Variant report

Variant	rs10743371
Chromosome Location	chr12:20550458-20550459
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10770647	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10770648	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10841503	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10841506	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11045209	0.94[ASN][1000 genomes]
rs11045210	0.95[ASN][1000 genomes]
rs11045219	0.89[EUR][1000 genomes]
rs12299821	0.85[ASN][1000 genomes]
rs1444642	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1899909	0.86[EUR][1000 genomes]
rs61246087	0.82[EUR][1000 genomes]
rs61911356	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61911357	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048067	chr12:20363755-20874845	Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv541408	chr12:20363755-20874845	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1046870	chr12:20509914-20711535	Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
4	nsv541409	chr12:20509914-20711535	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
5	nsv1042315	chr12:20531641-20629866	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20538200-20558000	Weak transcription	Left Ventricle	heart
2	chr12:20542600-20566200	Weak transcription	Aorta	Aorta
3	chr12:20543000-20551000	Weak transcription	A549	lung
4	chr12:20544000-20556000	Weak transcription	Osteobl	bone
5	chr12:20544800-20555800	Weak transcription	Colon Smooth Muscle	Colon
6	chr12:20548200-20550800	Weak transcription	Hela-S3	cervix
7	chr12:20548200-20556000	Weak transcription	Fetal Intestine Large	intestine
8	chr12:20549000-20553200	Weak transcription	Fetal Intestine Small	intestine
9	chr12:20549000-20555000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:20549400-20555600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr12:20549400-20557800	Weak transcription	Right Ventricle	heart
12	chr12:20550400-20551600	Enhancers	HUVEC	blood vessel
13	chr12:20550400-20552800	Weak transcription	Fetal Heart	heart
14	chr12:20550400-20568200	Weak transcription	Rectal Mucosa Donor 31	rectum

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

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