Variant report

Variant	rs73849676
Chromosome Location	chr3:103091004-103091005
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs56330410	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002641	chr3:102978116-103272330	Enhancers ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
2	nsv877238	chr3:103035266-103127478	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
3	nsv948426	chr3:103046716-103952548	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv949251	chr3:103046716-103977037	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
5	nsv527886	chr3:103048891-103989893	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
6	nsv877239	chr3:103071274-103119526	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	nsv965341	chr3:103072405-103099613	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	nsv877240	chr3:103073515-103097277	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3462262	chr3:103078769-103097124	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3462265	chr3:103078787-103097137	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3462264	chr3:103078834-103097116	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3462266	chr3:103078940-103097020	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	nsv877241	chr3:103090241-103151043	Enhancers Weak transcription Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:103089800-103091400	Enhancers	Fetal Brain Female	brain

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

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