Variant report

Variant	rs6919623
Chromosome Location	chr6:70000505-70000506
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11962594	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11965487	1.00[CEU][hapmap]
rs1283464	1.00[CEU][hapmap]
rs1293154	0.90[EUR][1000 genomes]
rs1297415	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs13195278	1.00[CEU][hapmap]
rs1410699	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs1512234	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16900620	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1706838	0.88[EUR][1000 genomes]
rs1928060	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs314208	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs314216	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs35829738	0.97[EUR][1000 genomes]
rs701655	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs701656	0.89[CEU][hapmap];0.95[EUR][1000 genomes]
rs71557617	0.92[EUR][1000 genomes]
rs7751967	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs779455	0.90[CEU][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs779459	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs779461	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs779462	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs779467	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs779470	0.90[CEU][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs779474	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs779483	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs779487	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs779492	0.81[EUR][1000 genomes]
rs9346271	0.88[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	nsv886137	chr6:69684850-70095690	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv432919	chr6:69873179-70221322	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv886139	chr6:69979989-70041922	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:69991000-70003400	Weak transcription	Fetal Brain Female	brain
2	chr6:69991800-70002800	Weak transcription	Brain Angular Gyrus	brain
3	chr6:69994400-70015400	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr6:69999400-70000600	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr6:70000000-70007600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr6:70000200-70000600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:70000200-70009000	Weak transcription	Fetal Brain Male	brain

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