Variant report

Variant	rs11755481
Chromosome Location	chr6:110342563-110342564
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11755985	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11756044	0.87[AMR][1000 genomes]
rs11757982	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56131993	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56272355	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72934012	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7751796	0.80[EUR][1000 genomes]
rs7772041	0.80[EUR][1000 genomes]
rs879134	0.80[AMR][1000 genomes]

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	nsv1019690	chr6:110102601-110360778	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1017642	chr6:110252276-110386453	Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv538417	chr6:110252276-110386453	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110340600-110343000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr6:110341400-110342600	Enhancers	Primary T cells from cord blood	blood
3	chr6:110341400-110342600	Enhancers	Primary hematopoietic stem cells	blood
4	chr6:110341400-110342800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr6:110341400-110343000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr6:110341600-110342600	Enhancers	Primary B cells from peripheral blood	blood
7	chr6:110341600-110342600	Enhancers	Dnd41	blood
8	chr6:110341600-110343000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr6:110341800-110342600	Enhancers	Primary T cells fromperipheralblood	blood
10	chr6:110341800-110342600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr6:110342000-110342600	Enhancers	Primary B cells from cord blood	blood
12	chr6:110342000-110342600	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr6:110342000-110342600	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr6:110342000-110342800	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr6:110342200-110342600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
16	chr6:110342400-110343000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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