Variant report

Variant	rs2133034
Chromosome Location	chr3:111294819-111294820
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1533270	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2175748	1.00[AMR][1000 genomes]
rs4682053	1.00[AMR][1000 genomes]
rs4682277	1.00[AMR][1000 genomes]
rs59853606	1.00[AMR][1000 genomes]
rs6777041	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs72939556	1.00[AMR][1000 genomes]
rs72939590	1.00[AMR][1000 genomes]
rs72944098	1.00[AMR][1000 genomes]
rs9288927	1.00[CHB][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	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv997756	chr3:111226058-111376585	Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111288400-111296000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr3:111288600-111296600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr3:111290000-111295000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr3:111290000-111297200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr3:111291000-111295800	Weak transcription	Fetal Thymus	thymus
6	chr3:111291000-111297000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr3:111291000-111297200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr3:111291200-111295800	Weak transcription	Thymus	Thymus
9	chr3:111291800-111298000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr3:111292000-111297600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr3:111292400-111297200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr3:111293600-111296400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr3:111294200-111296000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr3:111294200-111296400	Genic enhancers	Dnd41	blood
15	chr3:111294200-111302000	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr3:111294600-111295600	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr3:111294800-111295800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr3:111294800-111295800	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr3:111294800-111296000	Weak transcription	Primary T cells from cord blood	blood

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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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