Variant report

Variant	rs7856321
Chromosome Location	chr9:21476328-21476329
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10757222	0.89[JPT][hapmap]
rs10811546	0.82[JPT][hapmap]
rs10811551	0.90[JPT][hapmap]
rs10965003	0.85[AFR][1000 genomes]
rs10965014	0.88[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs10965015	0.87[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs10965020	0.87[JPT][hapmap]
rs10965021	1.00[JPT][hapmap]
rs10965022	0.81[JPT][hapmap]
rs10965023	1.00[JPT][hapmap]
rs10965026	0.90[JPT][hapmap]
rs12236551	0.82[JPT][hapmap]
rs1412397	0.82[JPT][hapmap]
rs56871984	0.85[EUR][1000 genomes]
rs57868054	0.85[EUR][1000 genomes]
rs57922867	0.87[EUR][1000 genomes]
rs60931924	0.93[EUR][1000 genomes]
rs6475536	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7030231	0.82[JPT][hapmap]
rs7048384	0.82[JPT][hapmap]
rs7861480	0.87[AFR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892724	chr9:20690244-21517302	Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	153 gene(s)	inside rSNPs	diseases
2	esv2752289	chr9:21361957-21499624	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv466297	chr9:21391698-21507589	Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv613758	chr9:21391698-21507589	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1030064	chr9:21455760-21524674	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA miRNA	111 gene(s)	inside rSNPs	diseases
6	nsv613759	chr9:21455814-21492506	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1020445	chr9:21464962-21524162	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA miRNA	109 gene(s)	inside rSNPs	diseases
8	nsv1020232	chr9:21464962-21524999	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA miRNA	110 gene(s)	inside rSNPs	diseases
9	nsv892740	chr9:21471499-21551513	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA miRNA	110 gene(s)	inside rSNPs	diseases
10	nsv1031432	chr9:21472601-21608774	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	122 gene(s)	inside rSNPs	diseases
11	nsv540085	chr9:21472601-21608774	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	122 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21454800-21481600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr9:21455200-21481000	Weak transcription	NHDF-Ad	bronchial
3	chr9:21455800-21481000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr9:21456000-21476600	Weak transcription	NHLF	lung
5	chr9:21463000-21502200	Weak transcription	HSMM	muscle
6	chr9:21466000-21527600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:21467000-21478600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:21468600-21477600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr9:21469000-21476400	Weak transcription	A549	lung
10	chr9:21469000-21478200	Strong transcription	Osteobl	bone
11	chr9:21469200-21477800	Strong transcription	HMEC	breast
12	chr9:21470200-21477800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:21471400-21477800	Strong transcription	NH-A	brain
14	chr9:21471600-21505600	Weak transcription	HUVEC	blood vessel
15	chr9:21473800-21476400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr9:21474400-21477000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr9:21475000-21481000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr9:21475000-21485600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr9:21475400-21478000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr9:21475400-21481000	Weak transcription	NHEK	skin
21	chr9:21475800-21476600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr9:21475800-21477400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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