Variant report

Variant	rs10951385
Chromosome Location	chr7:33369088-33369089
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10230991	1.00[YRI][hapmap]
rs10235943	1.00[YRI][hapmap]
rs10236358	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs10239609	1.00[YRI][hapmap]
rs10243590	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs10245418	1.00[YRI][hapmap]
rs10250312	1.00[YRI][hapmap]
rs10252552	1.00[YRI][hapmap]
rs10252927	1.00[YRI][hapmap]
rs10252935	1.00[YRI][hapmap]
rs10253352	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs10253574	1.00[YRI][hapmap]
rs10257379	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs10259513	1.00[YRI][hapmap]
rs10259674	1.00[YRI][hapmap]
rs10266641	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs10267370	1.00[YRI][hapmap]
rs10269511	1.00[YRI][hapmap]
rs10270137	0.91[AFR][1000 genomes]
rs10272446	0.91[AFR][1000 genomes]
rs10275832	1.00[YRI][hapmap]
rs10276929	1.00[YRI][hapmap]
rs12333380	1.00[YRI][hapmap]
rs12334131	1.00[YRI][hapmap]
rs12672071	1.00[YRI][hapmap]
rs12672496	1.00[YRI][hapmap]
rs28465518	0.91[AFR][1000 genomes]
rs28478218	0.91[AFR][1000 genomes]
rs28564487	0.91[AFR][1000 genomes]
rs28622379	0.91[AFR][1000 genomes]
rs3779240	1.00[YRI][hapmap]
rs4298411	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs6969260	1.00[YRI][hapmap]
rs6974593	1.00[YRI][hapmap]
rs9785054	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606610	chr7:33218763-33486316	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1016416	chr7:33241443-33559477	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv916660	chr7:33272493-33506384	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33355200-33419600	Weak transcription	Primary T cells from cord blood	blood
2	chr7:33362200-33404400	Weak transcription	Ovary	ovary
3	chr7:33362200-33404800	Weak transcription	Fetal Lung	lung
4	chr7:33364400-33370400	Weak transcription	Fetal Stomach	stomach
5	chr7:33366600-33384000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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