Variant report

Variant	rs7994611
Chromosome Location	chr13:38621772-38621773
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1073835	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1360921	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1360922	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1360923	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1538154	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1961338	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1981172	0.89[ASN][1000 genomes]
rs2323729	0.81[EUR][1000 genomes]
rs4262828	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4539457	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4941883	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56320674	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61956980	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6563579	0.92[CEU][hapmap]
rs7326544	0.89[ASN][1000 genomes]
rs7334221	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7336538	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7336728	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7336735	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7336857	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7994309	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8002822	0.92[CEU][hapmap]
rs9315543	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9532147	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9548172	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9566295	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9576428	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9576429	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv869125	chr13:38550449-39132813	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv949406	chr13:38561474-39033484	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv899999	chr13:38582178-38636966	ZNF genes & repeats Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv900000	chr13:38608928-38710260	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv900001	chr13:38619750-38710260	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7994611	LINC00571	cis	Thyroid	GTEx

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38620200-38622400	Weak transcription	Ovary	ovary
2	chr13:38620200-38633600	Weak transcription	Pancreas	Pancrea
3	chr13:38621600-38624800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr13:38621600-38626200	Weak transcription	Liver	Liver
5	chr13:38621600-38633600	Weak transcription	Aorta	Aorta

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