Variant report

Variant	rs7281637
Chromosome Location	chr21:37974794-37974795
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:37972910..37975712-chr21:37978328..37980849,2	MCF-7	breast:
2	chr21:37797860..37800286-chr21:37973474..37976401,2	MCF-7	breast:
3	chr21:37970149..37972535-chr21:37972835..37974907,2	K562	blood:
4	chr21:37973420..37975043-chr21:37996316..37998941,2	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs11910519	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12386295	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12482375	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13047871	0.82[ASN][1000 genomes]
rs13050224	0.84[ASN][1000 genomes]
rs13050577	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13051386	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2032150	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2409822	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2734392	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2734393	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2835390	0.82[ASN][1000 genomes]
rs2835394	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2835397	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2835399	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2835400	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2845783	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2845784	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2845785	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2845786	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2850085	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34053958	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34521064	0.93[ASN][1000 genomes]
rs377483	0.82[ASN][1000 genomes]
rs377777	0.82[ASN][1000 genomes]
rs382620	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs386394	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs386752	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs390584	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs400731	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs405828	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs412510	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs419513	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs420352	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs420885	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs426275	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs430159	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs431741	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs432137	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs432294	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs432706	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4372989	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs437724	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs438064	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs438492	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs441389	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs441524	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs450932	0.81[ASN][1000 genomes]
rs4528850	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7275576	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7280686	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs876780	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9305597	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9983642	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834090	chr21:37812545-38009542	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1064290	chr21:37878964-37983133	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv2762111	chr21:37967924-38023546	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv979509	chr21:37973119-37976589	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:37970600-37974800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr21:37973400-37975200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr21:37973600-37976400	Enhancers	Primary T cells fromperipheralblood	blood
4	chr21:37973600-37978800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr21:37974200-37975200	Enhancers	Primary T cells from cord blood	blood
6	chr21:37974200-37975200	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr21:37974200-37976000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr21:37974600-37977200	Enhancers	Primary T helper naive cells from peripheral blood	blood

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