Variant report

Variant	rs13191240
Chromosome Location	chr6:69675459-69675460
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1007921	1.00[CHB][hapmap]
rs10485436	1.00[YRI][hapmap]
rs13191563	1.00[JPT][hapmap]
rs13191706	1.00[CEU][hapmap];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13194716	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13197569	1.00[JPT][hapmap]
rs13204994	0.83[AMR][1000 genomes]
rs13205016	1.00[JPT][hapmap]
rs13205140	1.00[JPT][hapmap]
rs13207774	0.87[YRI][hapmap]
rs13219339	1.00[JPT][hapmap]
rs13219669	1.00[JPT][hapmap]
rs16900400	1.00[JPT][hapmap]
rs2200088	1.00[JPT][hapmap]
rs34470831	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34526480	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34617600	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3734465	1.00[CHB][hapmap]
rs3757045	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs3798978	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3798980	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3798996	1.00[JPT][hapmap]
rs3799007	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3799021	1.00[CHB][hapmap]
rs3799023	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3799030	1.00[CHB][hapmap]
rs3823061	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs6455309	1.00[CHB][hapmap]
rs6903686	1.00[JPT][hapmap]
rs6908180	1.00[JPT][hapmap]
rs6919909	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6934473	1.00[JPT][hapmap]
rs71555397	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7760307	1.00[CHB][hapmap]
rs7761270	1.00[JPT][hapmap]
rs7764479	1.00[CHB][hapmap]
rs7767118	1.00[CHB][hapmap];1.00[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv5338	chr6:69670701-69701360	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:69645600-69679000	Weak transcription	Fetal Brain Female	brain
2	chr6:69646000-69685000	Weak transcription	Fetal Lung	lung
3	chr6:69646200-69677200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr6:69647600-69677800	Weak transcription	Brain Anterior Caudate	brain
5	chr6:69652200-69684600	Weak transcription	Brain Angular Gyrus	brain
6	chr6:69654400-69677600	Weak transcription	Brain Hippocampus Middle	brain
7	chr6:69655000-69677600	Weak transcription	Brain Substantia Nigra	brain
8	chr6:69666600-69677800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr6:69670200-69685000	Weak transcription	Brain Germinal Matrix	brain
10	chr6:69672200-69675800	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr6:69673200-69680600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr6:69674000-69677800	Weak transcription	Brain Cingulate Gyrus	brain
13	chr6:69675000-69676400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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