Variant report

Variant	rs56758577
Chromosome Location	chr11:4037548-4037549
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11030046	1.00[EUR][1000 genomes]
rs12271827	1.00[EUR][1000 genomes]
rs12289770	1.00[EUR][1000 genomes]
rs2228121	1.00[EUR][1000 genomes]
rs7104387	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7131500	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74050924	1.00[EUR][1000 genomes]
rs74050926	1.00[EUR][1000 genomes]
rs7928229	1.00[EUR][1000 genomes]
rs7940082	1.00[EUR][1000 genomes]

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	nsv1046065	chr11:3808818-4049150	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv540909	chr11:3808818-4049150	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv896896	chr11:4010409-4185595	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1042719	chr11:4017541-4101609	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4017400-4041400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr11:4017600-4043400	Weak transcription	Primary B cells from cord blood	blood
3	chr11:4020800-4037600	Weak transcription	Pancreas	Pancrea
4	chr11:4020800-4045000	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr11:4021000-4043600	Weak transcription	Thymus	Thymus
6	chr11:4021000-4044200	Weak transcription	Fetal Thymus	thymus
7	chr11:4021000-4044400	Weak transcription	Dnd41	blood
8	chr11:4028800-4043400	Weak transcription	Primary T cells from cord blood	blood
9	chr11:4029000-4041400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr11:4030000-4037600	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr11:4030200-4044800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr11:4034000-4037600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr11:4036600-4040800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:4037000-4039200	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr11:4037200-4045000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr11:4037400-4037800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr11:4037400-4040000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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