Variant report

Variant	rs17354984
Chromosome Location	chr7:21782263-21782264
allele	C/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:14)

rs_ID	r²[population]
rs10156149	1.00[CEU][hapmap]
rs10485974	1.00[YRI][hapmap]
rs12672447	1.00[CEU][hapmap]
rs16872905	1.00[CEU][hapmap]
rs17145154	1.00[CEU][hapmap]
rs17145200	1.00[CEU][hapmap]
rs17145214	1.00[CEU][hapmap]
rs17145249	1.00[CEU][hapmap]
rs17145261	1.00[CEU][hapmap]
rs17145274	1.00[CEU][hapmap]
rs2072222	1.00[CEU][hapmap]
rs2965362	1.00[CEU][hapmap]
rs2965363	1.00[CEU][hapmap]
rs7796262	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018133	chr7:21740118-22055283	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1016063	chr7:21740433-21808410	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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