Variant report

Variant	rs17144018
Chromosome Location	chr7:71294853-71294854
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs12530530	1.00[CEU][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs12536303	0.87[EUR][1000 genomes]
rs12537319	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12540791	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs12668764	0.87[EUR][1000 genomes]
rs12669224	0.87[EUR][1000 genomes]
rs12670326	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12671022	1.00[CEU][hapmap];0.81[TSI][hapmap];0.93[EUR][1000 genomes]
rs12672393	0.89[EUR][1000 genomes]
rs12699101	0.82[CEU][hapmap]
rs12699103	0.94[EUR][1000 genomes]
rs12699104	0.94[EUR][1000 genomes]
rs12699108	0.87[EUR][1000 genomes]
rs12699109	0.85[EUR][1000 genomes]
rs12699110	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs12699111	0.87[EUR][1000 genomes]
rs13224623	1.00[CEU][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs13225975	1.00[CEU][hapmap]
rs13227550	1.00[CEU][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs13229166	0.87[EUR][1000 genomes]
rs13229182	1.00[CEU][hapmap]
rs13230689	0.87[EUR][1000 genomes]
rs13235673	1.00[CEU][hapmap]
rs13239349	0.87[EUR][1000 genomes]
rs13241833	1.00[CEU][hapmap];0.90[TSI][hapmap]
rs13243279	1.00[CEU][hapmap]
rs17137575	1.00[CEU][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs17137582	0.87[EUR][1000 genomes]
rs17137587	0.87[EUR][1000 genomes]
rs17144069	0.87[EUR][1000 genomes]
rs17144079	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs17144089	0.87[EUR][1000 genomes]
rs17144092	0.87[EUR][1000 genomes]
rs17144104	1.00[CEU][hapmap]
rs17144122	1.00[CEU][hapmap]
rs1859554	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs2903599	0.87[EUR][1000 genomes]
rs34038314	0.94[EUR][1000 genomes]
rs34058852	0.94[EUR][1000 genomes]
rs34141892	0.85[EUR][1000 genomes]
rs34163271	0.87[EUR][1000 genomes]
rs35066942	0.85[EUR][1000 genomes]
rs35087986	0.94[EUR][1000 genomes]
rs35296889	0.87[EUR][1000 genomes]
rs35316447	0.87[EUR][1000 genomes]
rs35341095	0.87[EUR][1000 genomes]
rs35412752	0.94[EUR][1000 genomes]
rs35490556	0.87[EUR][1000 genomes]
rs35708009	0.87[EUR][1000 genomes]
rs4717617	0.87[EUR][1000 genomes]
rs4719181	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs4719182	0.87[CEU][hapmap];0.87[EUR][1000 genomes]
rs4719183	1.00[CEU][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs4719184	0.87[EUR][1000 genomes]
rs4719185	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs4719186	1.00[CEU][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs4719188	1.00[CEU][hapmap];0.90[TSI][hapmap]
rs55748356	0.85[EUR][1000 genomes]
rs56251697	0.82[EUR][1000 genomes]
rs59305596	0.89[EUR][1000 genomes]
rs66463629	0.94[EUR][1000 genomes]
rs67719947	0.89[EUR][1000 genomes]
rs67740126	0.94[EUR][1000 genomes]
rs71551228	0.87[EUR][1000 genomes]
rs71551229	0.87[EUR][1000 genomes]
rs71551230	0.82[EUR][1000 genomes]
rs71551231	0.87[EUR][1000 genomes]
rs71551232	0.87[EUR][1000 genomes]
rs721235	1.00[CEU][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs7806602	1.00[CEU][hapmap];1.00[TSI][hapmap];0.87[EUR][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	nsv1026896	chr7:71003462-71721516	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1027496	chr7:71162362-71575116	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916220	chr7:71200006-71708048	Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71275800-71300000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:71292200-71299600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:71292200-71307000	Weak transcription	Fetal Thymus	thymus
4	chr7:71292400-71308200	Weak transcription	Thymus	Thymus
5	chr7:71292400-71308800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:71294400-71295000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr7:71294400-71295000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr7:71294800-71301000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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