Variant report

Variant	rs2691442
Chromosome Location	chr1:58002530-58002531
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10889048	0.83[CHB][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10889049	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10889050	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10889051	0.83[ASN][1000 genomes]
rs11207058	0.83[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1341319	0.83[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1357782	0.84[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1524713	0.83[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1524714	0.83[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1524715	0.83[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1524716	0.84[CEU][hapmap];0.83[CHB][hapmap];0.93[JPT][hapmap];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1572943	0.84[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1880443	0.83[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1949830	0.84[CEU][hapmap];0.83[CHB][hapmap];0.93[JPT][hapmap];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1949831	0.92[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1949832	0.83[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2264665	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs2406068	1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2691440	1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2691441	0.84[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2691446	0.83[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2691456	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2691470	0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2793625	0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2793626	0.84[CEU][hapmap];0.93[JPT][hapmap];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4912259	0.84[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817216	chr1:57801783-58130775	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1001771	chr1:57837089-58068175	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv870908	chr1:57884310-58037783	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1012555	chr1:57950355-58103389	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv870802	chr1:57965114-58037031	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1015057	chr1:57976993-58793962	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv530017	chr1:58002290-58669736	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57989200-58012200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:58000800-58003800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:58000800-58003800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr1:58001600-58002600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr1:58001600-58002600	Enhancers	Fetal Muscle Leg	muscle
6	chr1:58001800-58002600	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr1:58002200-58002800	Enhancers	Psoas Muscle	Psoas
8	chr1:58002200-58007800	Weak transcription	Stomach Mucosa	stomach
9	chr1:58002400-58002600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:58002400-58002800	Enhancers	Skeletal Muscle Male	skeletal muscle

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