Variant report

Variant	rs12007684
Chromosome Location	chrX:91551621-91551622
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12011840	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];1.00[TSI][hapmap]
rs12014732	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs12014801	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs12116136	0.82[YRI][hapmap]
rs12556087	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs12556336	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12556807	0.90[YRI][hapmap]
rs12557070	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs12557973	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs12559956	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12560026	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[TSI][hapmap]
rs5984917	1.00[CEU][hapmap]
rs5984918	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[TSI][hapmap]
rs6615351	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs6615352	1.00[CEU][hapmap]
rs6615374	1.00[CEU][hapmap]

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	nsv432350	chrX:91158935-91590765	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv532885	chrX:91428554-92377178	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv1001030	chrX:91539006-92375367	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv15966	chrX:91540570-92371792	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region lncRNA	5 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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