Variant report

Variant	rs490005
Chromosome Location	chr9:22020493-22020494
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10115049	1.00[ASN][1000 genomes]
rs10120688	0.81[ASN][1000 genomes]
rs10738605	0.87[ASN][1000 genomes]
rs10757263	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10757264	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10757265	0.87[ASN][1000 genomes]
rs10757266	0.87[ASN][1000 genomes]
rs10757267	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs10811640	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10811643	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10811644	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10811645	0.84[AFR][1000 genomes]
rs10965212	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10965215	1.00[ASN][1000 genomes]
rs10965219	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1333036	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1360590	0.87[ASN][1000 genomes]
rs1591136	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2106119	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2106120	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2151280	0.89[ASN][1000 genomes]
rs2383204	0.87[ASN][1000 genomes]
rs2811712	0.86[AFR][1000 genomes]
rs3218002	0.82[AFR][1000 genomes]
rs3218005	0.86[AFR][1000 genomes]
rs3218007	0.86[AFR][1000 genomes]
rs3218012	0.81[EUR][1000 genomes]
rs496892	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4977753	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs504318	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs567453	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs581876	0.90[ASN][1000 genomes]
rs643319	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7027048	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7027950	0.87[ASN][1000 genomes]
rs7028570	0.87[ASN][1000 genomes]
rs7035484	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7044859	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7049105	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs944799	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529609	chr9:21708371-22537069	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv8426	chr9:21763810-22176200	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1018514	chr9:21944275-22075326	Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv892746	chr9:21953137-22028801	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv892747	chr9:21984661-22068646	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv531617	chr9:21985057-22809676	Genic enhancers Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:22009800-22030200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:22009800-22037000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr9:22010000-22029400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:22010000-22029800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr9:22013800-22024400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:22017000-22027000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr9:22017800-22024000	Weak transcription	Dnd41	blood
8	chr9:22019800-22024400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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