Variant report

Variant	rs6671529
Chromosome Location	chr1:79843800-79843801
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11162698	1.00[EUR][1000 genomes]
rs11162708	1.00[EUR][1000 genomes]
rs12067404	1.00[EUR][1000 genomes]
rs12089887	1.00[EUR][1000 genomes]
rs12091688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12092037	1.00[EUR][1000 genomes]
rs12092854	1.00[EUR][1000 genomes]
rs12095310	1.00[EUR][1000 genomes]
rs13376313	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17098650	0.90[EUR][1000 genomes]
rs17103122	1.00[EUR][1000 genomes]
rs17103225	0.90[EUR][1000 genomes]
rs17103302	0.86[EUR][1000 genomes]
rs17103311	0.86[EUR][1000 genomes]
rs28762700	0.86[EUR][1000 genomes]
rs3015007	0.90[EUR][1000 genomes]
rs3953575	0.90[EUR][1000 genomes]
rs57263150	1.00[EUR][1000 genomes]
rs58319353	1.00[EUR][1000 genomes]
rs58925724	1.00[EUR][1000 genomes]
rs58937668	0.86[EUR][1000 genomes]
rs6658868	1.00[EUR][1000 genomes]
rs6661647	1.00[EUR][1000 genomes]
rs6686663	1.00[EUR][1000 genomes]
rs6695364	0.86[EUR][1000 genomes]
rs72946533	1.00[EUR][1000 genomes]
rs7541121	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491784	chr1:79146141-79853482	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv870657	chr1:79701220-79890774	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv830337	chr1:79791879-79913241	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv546633	chr1:79794719-79877035	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv871649	chr1:79807447-79924175	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1004014	chr1:79811049-80042309	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv462150	chr1:79835066-79873161	Enhancers Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv546634	chr1:79835066-79873161	Weak transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv462161	chr1:79835066-79877035	Enhancers Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv462173	chr1:79835066-79877035	Enhancers Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv470721	chr1:79835066-79877035	Enhancers Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv546635	chr1:79835066-79877035	Enhancers Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79842400-79844200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr1:79842800-79844000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr1:79843600-79843800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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