Variant report

Variant	rs12510249
Chromosome Location	chr4:131097432-131097433
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10007855	0.93[ASN][1000 genomes]
rs10428377	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10428378	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10428487	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10857142	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12504004	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12504193	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12504988	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12506695	0.91[ASN][1000 genomes]
rs12507635	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12508592	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1602817	0.91[ASN][1000 genomes]
rs17050858	0.91[ASN][1000 genomes]
rs17050866	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17050867	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1845224	0.89[ASN][1000 genomes]
rs2391602	0.91[ASN][1000 genomes]
rs2893314	0.91[ASN][1000 genomes]
rs35396668	0.91[ASN][1000 genomes]
rs4863964	0.89[ASN][1000 genomes]
rs4863965	0.91[ASN][1000 genomes]
rs4864370	0.91[ASN][1000 genomes]
rs4864371	0.91[ASN][1000 genomes]
rs55830439	0.89[ASN][1000 genomes]
rs55875040	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55898536	0.91[ASN][1000 genomes]
rs55917330	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56058926	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56102048	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56138792	0.85[ASN][1000 genomes]
rs56291403	0.91[ASN][1000 genomes]
rs56370907	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56993070	0.91[ASN][1000 genomes]
rs57361902	0.88[ASN][1000 genomes]
rs57560215	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58014327	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58301705	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59386731	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59590770	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59669577	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60713285	0.91[ASN][1000 genomes]
rs60998307	0.91[ASN][1000 genomes]
rs61007864	0.91[ASN][1000 genomes]
rs66664915	0.91[ASN][1000 genomes]
rs66700617	0.91[ASN][1000 genomes]
rs66819704	0.91[ASN][1000 genomes]
rs66853091	0.91[ASN][1000 genomes]
rs66951606	0.91[ASN][1000 genomes]
rs66953717	0.91[ASN][1000 genomes]
rs66956392	0.91[ASN][1000 genomes]
rs66992044	0.91[ASN][1000 genomes]
rs67052396	0.91[ASN][1000 genomes]
rs67122917	0.91[ASN][1000 genomes]
rs67425927	0.91[ASN][1000 genomes]
rs67634627	0.91[ASN][1000 genomes]
rs67764870	0.88[ASN][1000 genomes]
rs68063814	0.91[ASN][1000 genomes]
rs6851893	0.91[ASN][1000 genomes]
rs72934696	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72934698	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv595416	chr4:130998472-131834405	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv2762461	chr4:131004382-131391658	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1025539	chr4:131033276-131728033	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv537253	chr4:131033276-131728033	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv830061	chr4:131064845-131228710	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv879937	chr4:131065136-131174088	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv1034250	chr4:131080340-131112576	Enhancers ZNF genes & repeats Weak transcription	lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:131096600-131099400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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