Variant report

Variant	rs297336
Chromosome Location	chr11:16400866-16400867
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10732463	0.93[AFR][1000 genomes]
rs10734241	0.93[AFR][1000 genomes]
rs10734243	0.93[AFR][1000 genomes]
rs10734244	0.93[AFR][1000 genomes]
rs10734245	0.93[AFR][1000 genomes]
rs10734246	0.93[AFR][1000 genomes]
rs1123186	0.93[AFR][1000 genomes]
rs1393925	0.93[AFR][1000 genomes]
rs1393929	0.93[AFR][1000 genomes]
rs1466927	0.93[AFR][1000 genomes]
rs1466928	0.93[AFR][1000 genomes]
rs1503451	0.93[AFR][1000 genomes]
rs2062813	0.93[AFR][1000 genomes]
rs2134611	0.93[AFR][1000 genomes]
rs2352237	0.93[AFR][1000 genomes]
rs2938283	0.93[AFR][1000 genomes]
rs297323	0.93[AFR][1000 genomes]
rs297329	0.93[AFR][1000 genomes]
rs4757396	0.93[AFR][1000 genomes]
rs60970479	0.93[AFR][1000 genomes]
rs6486289	0.93[AFR][1000 genomes]
rs7104395	0.93[AFR][1000 genomes]
rs7123022	0.93[AFR][1000 genomes]
rs7945381	0.93[AFR][1000 genomes]
rs959966	0.93[AFR][1000 genomes]
rs967423	0.93[AFR][1000 genomes]
rs967424	0.93[AFR][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	nsv529731	chr11:16122782-16468170	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv553566	chr11:16329009-16799044	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv832075	chr11:16391700-16490934	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr11:16388200-16414200	Weak transcription	Fetal Intestine Small	intestine
2	chr11:16397200-16402000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr11:16398200-16403000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:16399400-16404000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:16400600-16401000	Enhancers	Psoas Muscle	Psoas
6	chr11:16400600-16401400	Enhancers	K562	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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