Variant report

Variant	rs4011661
Chromosome Location	chr14:31717581-31717582
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10132373	0.80[EUR][1000 genomes]
rs10135213	0.81[EUR][1000 genomes]
rs10138200	0.81[EUR][1000 genomes]
rs10151563	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1041088	0.81[EUR][1000 genomes]
rs11626839	0.80[EUR][1000 genomes]
rs12889162	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs5024655	0.81[EUR][1000 genomes]
rs6571403	0.81[EUR][1000 genomes]
rs6571404	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7494025	0.81[EUR][1000 genomes]
rs9788563	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901587	chr14:31501505-31752664	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1050054	chr14:31501703-31733642	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	esv2830427	chr14:31639110-32000034	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv1050597	chr14:31711248-31904761	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 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	chr14:31707800-31730800	Weak transcription	Pancreas	Pancrea
2	chr14:31711600-31720400	Weak transcription	Duodenum Mucosa	Duodenum
3	chr14:31713800-31720800	Weak transcription	Fetal Intestine Small	intestine
4	chr14:31713800-31722200	Weak transcription	Lung	lung
5	chr14:31714200-31720200	Weak transcription	HepG2	liver
6	chr14:31714200-31720600	Weak transcription	A549	lung
7	chr14:31717400-31720400	Weak transcription	Stomach Mucosa	stomach

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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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