Variant report

Variant	rs2225181
Chromosome Location	chr9:15922325-15922326
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 133 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:131)

rs_ID	r²[population]
rs10733305	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs10738417	0.95[JPT][hapmap]
rs10738419	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs10738420	0.86[JPT][hapmap]
rs10756697	0.95[CHB][hapmap];0.81[JPT][hapmap]
rs10756704	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs10756709	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs10756710	0.85[CHB][hapmap];0.83[JPT][hapmap]
rs10756711	0.85[CHB][hapmap];0.83[JPT][hapmap]
rs10756714	0.91[JPT][hapmap]
rs10756715	0.95[JPT][hapmap]
rs10756720	0.86[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs10756721	0.86[ASN][1000 genomes]
rs10756722	0.91[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs10756726	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs10756728	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs10756729	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs10810439	0.95[CHB][hapmap]
rs10810446	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs10810455	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs10810461	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs10810462	0.80[CEU][hapmap];0.86[CHB][hapmap]
rs10810474	0.81[ASN][1000 genomes]
rs10810475	0.83[ASN][1000 genomes]
rs10810479	0.84[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs10810480	0.88[ASN][1000 genomes]
rs10810481	0.88[ASN][1000 genomes]
rs10810482	0.88[ASN][1000 genomes]
rs10810483	0.91[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs10810484	0.90[CHB][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs10810485	0.81[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs10810486	0.86[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs10810487	0.86[CHB][hapmap];0.82[JPT][hapmap];0.80[ASN][1000 genomes]
rs10810488	0.86[CHB][hapmap];0.81[JPT][hapmap];0.80[ASN][1000 genomes]
rs10810501	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs10810502	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs10810506	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs10810509	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs10962142	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs10962151	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs10962156	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs10962157	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs10962158	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs10962212	0.80[ASN][1000 genomes]
rs10962215	0.83[ASN][1000 genomes]
rs10962225	0.91[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs10962227	0.86[CHB][hapmap];0.82[JPT][hapmap];0.80[ASN][1000 genomes]
rs1169478	0.90[CEU][hapmap]
rs1169479	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs1169480	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs12378499	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs12379234	0.90[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs1328283	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs1328286	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AFR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1328288	0.91[CEU][hapmap];0.95[EUR][1000 genomes]
rs13287834	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs13292699	0.84[ASN][1000 genomes]
rs13296360	0.95[CHB][hapmap];0.81[JPT][hapmap]
rs13297383	0.80[ASN][1000 genomes]
rs1341732	0.85[CHB][hapmap];0.95[JPT][hapmap]
rs1341737	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs1341738	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs1359952	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1359953	0.96[CEU][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1410444	0.81[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs1410445	0.85[ASN][1000 genomes]
rs1410446	0.89[ASN][1000 genomes]
rs1539172	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs1539173	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs1592099	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs1927696	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1927697	0.88[ASN][1000 genomes]
rs1927698	0.91[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs2105315	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs2182936	0.84[ASN][1000 genomes]
rs2185663	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs2225182	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs2382540	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs2794634	0.86[CEU][hapmap];0.80[EUR][1000 genomes]
rs2794636	0.85[CEU][hapmap]
rs2794645	0.80[EUR][1000 genomes]
rs2794646	0.81[EUR][1000 genomes]
rs2794647	0.80[EUR][1000 genomes]
rs2987008	0.80[EUR][1000 genomes]
rs2987009	0.93[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes]
rs2987010	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs2987011	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs2987012	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs2987013	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs2987014	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs2987069	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs2987070	0.93[CEU][hapmap];0.88[EUR][1000 genomes]
rs2987071	0.83[CEU][hapmap];0.88[EUR][1000 genomes]
rs2987072	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs3008666	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs3008678	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3008681	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3008686	0.82[CEU][hapmap];0.89[EUR][1000 genomes]
rs3008747	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs3008748	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs3008749	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs3008753	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs4146290	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs4146291	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs4146293	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs4472620	0.81[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs4582646	0.91[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs4740624	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs4740628	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs4741535	0.95[CHB][hapmap];0.82[JPT][hapmap]
rs4741545	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs4741546	0.95[CHB][hapmap];0.82[JPT][hapmap]
rs4741548	0.83[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs4741552	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs4741553	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs6474967	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs6474974	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs7043770	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs735962	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs770191	0.82[CEU][hapmap];0.82[JPT][hapmap]
rs770211	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs770213	0.86[CEU][hapmap]
rs770215	0.82[CEU][hapmap]
rs7849380	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs7860528	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs7860755	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs7873776	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs950234	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs955369	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs961117	0.81[CHB][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs9650686	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2753625	chr9:15914055-15980320	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15918200-15930800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr9:15920000-15936000	Weak transcription	Ovary	ovary
3	chr9:15920600-15922800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:15920800-15922800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:15921600-15924800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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