Variant report

Variant	rs1379933
Chromosome Location	chr4:89801156-89801157
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10461165	0.92[ASN][1000 genomes]
rs1246629	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1246631	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1246632	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1246634	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1246642	0.92[EUR][1000 genomes]
rs12640274	0.92[ASN][1000 genomes]
rs1379932	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1458551	0.93[AFR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1563689	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2085600	0.93[ASN][1000 genomes]
rs2446300	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2446301	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2446303	0.81[AFR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2446304	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2464522	0.93[EUR][1000 genomes]
rs2464523	0.93[EUR][1000 genomes]
rs2464528	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2609255	0.93[AFR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2609258	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2609259	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2609261	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2609262	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2609264	0.81[AFR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2609265	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2609279	0.92[EUR][1000 genomes]
rs2609280	0.92[EUR][1000 genomes]
rs2704570	0.84[AFR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2704581	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2704582	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2704583	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2704587	0.93[EUR][1000 genomes]
rs2704604	0.93[EUR][1000 genomes]
rs2869952	1.00[AFR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28767574	0.92[ASN][1000 genomes]
rs2904255	0.81[ASN][1000 genomes]
rs56158219	0.85[ASN][1000 genomes]
rs6813090	0.81[AFR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6815970	0.93[AFR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7673818	0.90[EUR][1000 genomes]
rs9997652	0.86[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	nsv470051	chr4:89644931-90643144	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1009354	chr4:89725914-89985155	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv998651	chr4:89800245-89933445	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	nsv537175	chr4:89800245-89933445	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:89771000-89803200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:89782400-89801200	Weak transcription	Ovary	ovary
3	chr4:89787400-89801200	Weak transcription	Placenta	Placenta
4	chr4:89798800-89802800	Enhancers	HepG2	liver
5	chr4:89800000-89802800	Enhancers	Fetal Intestine Small	intestine
6	chr4:89800200-89802400	Enhancers	Fetal Intestine Large	intestine
7	chr4:89800600-89801800	Enhancers	Duodenum Mucosa	Duodenum
8	chr4:89800600-89801800	Enhancers	HSMMtube	muscle
9	chr4:89800600-89802600	Enhancers	Fetal Muscle Leg	muscle
10	chr4:89800600-89802600	Enhancers	Pancreas	Pancrea
11	chr4:89800800-89802400	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr4:89800800-89802400	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr4:89800800-89802600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:89801000-89803400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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