Variant report

Variant	rs17021737
Chromosome Location	chr3:28742304-28742305
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17021636	1.00[AMR][1000 genomes]
rs17021802	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3328565	chr3:27991169-28915035	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv916364	chr3:28468275-29146280	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1001920	chr3:28711075-28788920	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
4	esv3461677	chr3:28734924-28744248	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv3461678	chr3:28734963-28744223	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv3461679	chr3:28734990-28744180	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv3461680	chr3:28734990-28744180	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:28739600-28742400	Enhancers	HSMMtube	muscle
2	chr3:28740000-28743000	Enhancers	Pancreas	Pancrea
3	chr3:28740600-28743400	Weak transcription	Right Atrium	heart
4	chr3:28741600-28742400	Enhancers	Fetal Intestine Large	intestine
5	chr3:28742200-28742800	Enhancers	Aorta	Aorta

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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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