Variant report

Variant	rs6910974
Chromosome Location	chr6:45082169-45082170
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:45071425..45074350-chr6:45080859..45082948,2	MCF-7	breast:

Extended variants
information (count: 133 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:118)

rs_ID	r²[population]
rs1023089	0.85[AMR][1000 genomes]
rs1041332	0.92[CEU][hapmap];0.87[YRI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1080415	1.00[CEU][hapmap];0.87[YRI][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10807318	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10948197	0.81[YRI][hapmap]
rs10948198	0.84[AMR][1000 genomes]
rs11964325	0.80[YRI][hapmap]
rs11968042	0.89[AMR][1000 genomes]
rs12190261	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs12196818	0.81[YRI][hapmap]
rs12205071	0.87[AMR][1000 genomes]
rs12208023	0.81[YRI][hapmap];0.87[AMR][1000 genomes]
rs12208483	0.89[AMR][1000 genomes]
rs12214778	0.81[YRI][hapmap]
rs12529490	0.84[AMR][1000 genomes]
rs12529946	0.80[CEU][hapmap]
rs1284961	0.83[AMR][1000 genomes]
rs1284965	0.89[YRI][hapmap];0.83[AMR][1000 genomes]
rs1284969	0.83[YRI][hapmap];0.83[AMR][1000 genomes]
rs1284972	0.89[AMR][1000 genomes]
rs1284973	0.89[AMR][1000 genomes]
rs1284975	0.89[AMR][1000 genomes]
rs1284980	0.86[AMR][1000 genomes]
rs1284982	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1284983	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1284987	0.87[YRI][hapmap]
rs1284988	0.89[AMR][1000 genomes]
rs1284992	0.89[AMR][1000 genomes]
rs1285004	0.89[AMR][1000 genomes]
rs1285013	0.94[YRI][hapmap];0.83[AMR][1000 genomes]
rs1285014	0.94[YRI][hapmap];0.83[AMR][1000 genomes]
rs1285019	0.81[YRI][hapmap];0.83[AMR][1000 genomes]
rs1285022	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1285023	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1285026	1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs1290386	0.94[YRI][hapmap];0.83[AMR][1000 genomes]
rs1300126	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1304168	0.83[AMR][1000 genomes]
rs13202529	0.81[AMR][1000 genomes]
rs13207575	0.87[AMR][1000 genomes]
rs1324532	0.89[AMR][1000 genomes]
rs1324537	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1324540	0.81[AMR][1000 genomes]
rs1329710	0.84[CEU][hapmap];0.84[EUR][1000 genomes]
rs1329714	0.83[CHB][hapmap];0.85[AMR][1000 genomes]
rs1359336	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1360197	0.88[CEU][hapmap]
rs1411148	0.92[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1521355	0.84[CEU][hapmap]
rs1581777	0.81[AMR][1000 genomes]
rs1629542	0.94[YRI][hapmap];0.83[AMR][1000 genomes]
rs1748231	0.85[YRI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1748234	0.88[YRI][hapmap];0.87[AMR][1000 genomes]
rs1748235	0.87[AMR][1000 genomes]
rs1748237	0.82[AMR][1000 genomes]
rs1748242	0.83[YRI][hapmap];0.83[AMR][1000 genomes]
rs1797145	0.83[AMR][1000 genomes]
rs1797147	0.82[AMR][1000 genomes]
rs1886345	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1937046	0.88[AMR][1000 genomes]
rs1937047	0.88[AMR][1000 genomes]
rs1971482	0.80[AMR][1000 genomes]
rs2186062	0.89[YRI][hapmap];0.87[AMR][1000 genomes]
rs2396375	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3799986	0.84[CEU][hapmap]
rs3920903	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4373351	0.81[CEU][hapmap]
rs4398713	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4412189	0.87[AMR][1000 genomes]
rs4714836	0.86[AMR][1000 genomes]
rs56138724	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs608941	0.81[YRI][hapmap]
rs6458418	0.86[AMR][1000 genomes]
rs6458423	0.92[CEU][hapmap];0.89[YRI][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6458425	1.00[CEU][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6458427	0.92[CEU][hapmap];0.93[YRI][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6458430	0.83[AMR][1000 genomes]
rs67001335	0.80[EUR][1000 genomes]
rs6899378	0.89[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6901786	0.88[YRI][hapmap];0.83[AMR][1000 genomes]
rs6905396	0.89[YRI][hapmap];0.83[AMR][1000 genomes]
rs6919847	0.86[YRI][hapmap]
rs6922660	1.00[YRI][hapmap]
rs6923436	0.89[AMR][1000 genomes]
rs6938177	1.00[CEU][hapmap];0.84[YRI][hapmap];0.81[AMR][1000 genomes]
rs6938316	0.83[AMR][1000 genomes]
rs7738526	0.92[CEU][hapmap];0.89[YRI][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7739928	0.92[CEU][hapmap];0.94[YRI][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7742360	0.85[CEU][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7750380	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7758031	0.87[AMR][1000 genomes]
rs7760342	0.92[CEU][hapmap]
rs7763450	0.87[AMR][1000 genomes]
rs7764102	0.87[AMR][1000 genomes]
rs7767025	0.83[AMR][1000 genomes]
rs7769231	0.81[AMR][1000 genomes]
rs7775717	0.82[EUR][1000 genomes]
rs927658	0.89[YRI][hapmap];0.83[AMR][1000 genomes]
rs9296455	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9296458	0.83[AMR][1000 genomes]
rs9349309	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9349313	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9367214	0.92[CEU][hapmap];0.89[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9369529	0.85[AMR][1000 genomes]
rs9369530	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9369534	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9381361	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9381364	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9381365	0.92[CEU][hapmap];0.94[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9381373	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9395063	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9395065	0.86[AMR][1000 genomes]
rs9395088	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9463076	0.92[CEU][hapmap];0.94[YRI][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9472451	0.81[YRI][hapmap];0.81[AMR][1000 genomes]
rs964452	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs969211	0.83[YRI][hapmap];0.87[AMR][1000 genomes]
rs988147	0.87[YRI][hapmap];0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028393	chr6:44875558-45822335	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538211	chr6:44875558-45822335	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv1024370	chr6:44878053-45251451	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv885862	chr6:44890760-45083966	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv885863	chr6:44890760-45083966	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv885864	chr6:44890760-45198796	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1023018	chr6:44925393-45152912	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv538212	chr6:44925393-45152912	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1026728	chr6:45001948-45126730	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv538213	chr6:45001948-45126730	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv885865	chr6:45012223-45102025	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv492309	chr6:45020402-45233484	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
13	nsv528130	chr6:45056086-45083966	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv1032906	chr6:45069368-45212863	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
15	esv3449983	chr6:45081733-45082219	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6910974	SUPT3H	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45073400-45083600	Weak transcription	Pancreas	Pancrea
2	chr6:45076600-45082800	Weak transcription	Dnd41	blood
3	chr6:45077800-45083400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:45078400-45083400	Weak transcription	HSMM	muscle
5	chr6:45081200-45083200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:45081600-45084200	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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