Variant report

Variant	rs881031
Chromosome Location	chr3:69406856-69406857
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs12635365	0.85[ASN][1000 genomes]
rs13320477	0.86[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17005675	0.92[CEU][hapmap];0.93[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];0.97[LWK][hapmap];0.98[MKK][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17005685	0.85[CEU][hapmap];0.87[CHB][hapmap];0.87[CHD][hapmap];0.94[GIH][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17005687	0.85[CEU][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17005689	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17005691	0.85[CEU][hapmap];0.87[CHB][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17005694	0.85[CEU][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17005696	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17005699	0.85[CEU][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];0.90[GIH][hapmap];0.81[LWK][hapmap];0.89[MKK][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17005712	0.85[CEU][hapmap];0.86[MKK][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17005713	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17350402	0.93[CHB][hapmap];0.87[CHD][hapmap];0.97[GIH][hapmap];0.85[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17416638	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2314987	1.00[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2872808	1.00[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];0.82[YRI][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35298402	0.85[ASN][1000 genomes]
rs4241387	0.85[CEU][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4855388	0.81[GIH][hapmap]
rs4855391	0.83[ASN][1000 genomes]
rs4855394	0.83[CEU][hapmap];0.87[GIH][hapmap];0.81[LWK][hapmap];0.89[MKK][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs5026329	0.89[AMR][1000 genomes]
rs56052332	0.80[ASN][1000 genomes]
rs56138041	0.80[ASN][1000 genomes]
rs56653941	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56682655	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs57343519	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58156018	0.83[ASN][1000 genomes]
rs58937767	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs59605214	0.83[ASN][1000 genomes]
rs59683429	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs60969945	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72940765	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72940769	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72940771	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72940775	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72940779	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72940783	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72940785	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs964553	0.85[CEU][hapmap];0.91[AMR][1000 genomes];0.84[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	nsv1007730	chr3:69355932-69730587	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer 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	esv1800315	chr3:69374729-69414587	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv520818	chr3:69401248-69421495	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69400600-69412800	Weak transcription	Esophagus	oesophagus
2	chr3:69402200-69419000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr3:69402800-69413000	Weak transcription	Aorta	Aorta
4	chr3:69403000-69414800	Weak transcription	Lung	lung
5	chr3:69403800-69413000	Weak transcription	Thymus	Thymus
6	chr3:69404200-69408200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr3:69404600-69407000	Enhancers	Brain Cingulate Gyrus	brain
8	chr3:69405000-69408600	Weak transcription	HUVEC	blood vessel
9	chr3:69406000-69407000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr3:69406000-69407200	Enhancers	Hela-S3	cervix
11	chr3:69406000-69407200	Genic enhancers	NHEK	skin
12	chr3:69406000-69407400	Enhancers	HSMMtube	muscle
13	chr3:69406000-69407600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr3:69406000-69407600	Enhancers	HMEC	breast
15	chr3:69406200-69407200	Enhancers	Brain Anterior Caudate	brain
16	chr3:69406200-69407400	Enhancers	Brain Hippocampus Middle	brain
17	chr3:69406200-69407600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr3:69406200-69407600	Enhancers	Fetal Lung	lung
19	chr3:69406200-69408000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr3:69406200-69408000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr3:69406400-69407400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr3:69406600-69407200	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr3:69406600-69408000	Weak transcription	Fetal Thymus	thymus
24	chr3:69406600-69412800	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr3:69406800-69407000	Enhancers	HSMM	muscle
26	chr3:69406800-69409000	Weak transcription	Dnd41	blood
27	chr3:69406800-69413000	Weak transcription	Brain Substantia Nigra	brain
28	chr3:69406800-69413400	Weak transcription	Brain Angular Gyrus	brain

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