Variant report

Variant	rs10751100
Chromosome Location	chr11:83610835-83610836
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10792696	0.88[AFR][1000 genomes]
rs10898166	1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs10898168	0.92[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10898175	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10898177	0.82[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10898178	0.85[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11233771	0.81[CEU][hapmap];0.95[YRI][hapmap];0.90[AFR][1000 genomes]
rs11233776	0.90[YRI][hapmap];0.90[AFR][1000 genomes]
rs11537255	0.85[ASN][1000 genomes]
rs1400315	0.96[CHB][hapmap];0.96[JPT][hapmap];0.94[ASN][1000 genomes]
rs1483393	0.85[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1878265	0.91[CHB][hapmap];0.96[JPT][hapmap];0.91[ASN][1000 genomes]
rs2090372	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2102784	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7112497	0.93[ASN][1000 genomes]
rs7112521	0.81[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[YRI][hapmap];0.94[ASN][1000 genomes]
rs7927301	0.87[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7933375	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7933528	1.00[CHB][hapmap];0.91[JPT][hapmap];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7939073	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv468765	chr11:83591584-83620940	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv555607	chr11:83591584-83620940	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83607000-83611400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr11:83607200-83628800	Weak transcription	Brain Angular Gyrus	brain
3	chr11:83608400-83620800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr11:83608400-83634600	Weak transcription	Brain Hippocampus Middle	brain
5	chr11:83608800-83629400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr11:83609200-83616600	Weak transcription	Pancreas	Pancrea

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