Variant report

Variant	rs7795776
Chromosome Location	chr7:10819778-10819779
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:10810774..10813337-chr7:10818545..10820723,2	K562	blood:
2	chr7:10818173..10820348-chr7:10835092..10837253,2	K562	blood:
3	chr7:10768715..10771271-chr7:10816725..10820425,4	K562	blood:
4	chr7:10818699..10822020-chr7:10830372..10832359,3	K562	blood:
5	chr7:10781219..10782750-chr7:10819283..10821233,2	K562	blood:
6	chr7:10809717..10814120-chr7:10815612..10822714,11	K562	blood:
7	chr7:10778744..10781099-chr7:10818958..10821486,2	K562	blood:

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10230225	0.93[ASN][1000 genomes]
rs10230296	0.95[ASN][1000 genomes]
rs10233178	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10235207	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10238503	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10241830	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10250526	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10258847	0.93[ASN][1000 genomes]
rs10259141	0.93[ASN][1000 genomes]
rs10259958	0.81[ASN][1000 genomes]
rs10264572	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10268146	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10268469	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10272459	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10276033	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10276038	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10278489	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10486094	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10486096	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs10486100	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10950313	0.95[ASN][1000 genomes]
rs10950314	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11971102	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11976168	0.97[ASN][1000 genomes]
rs11978409	0.94[ASN][1000 genomes]
rs12670938	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12671358	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12671384	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17163474	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17163529	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17163540	0.96[ASN][1000 genomes]
rs2189534	0.93[ASN][1000 genomes]
rs2189538	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2189539	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2189543	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs28681162	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2882976	0.80[ASN][1000 genomes]
rs4289707	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4720904	0.80[ASN][1000 genomes]
rs4720905	0.80[ASN][1000 genomes]
rs56137539	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57599855	0.96[ASN][1000 genomes]
rs59864617	0.92[ASN][1000 genomes]
rs62454232	0.96[ASN][1000 genomes]
rs62454237	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6460748	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6944034	0.98[ASN][1000 genomes]
rs6944274	0.93[ASN][1000 genomes]
rs6944330	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6947809	0.87[ASN][1000 genomes]
rs6948792	0.96[ASN][1000 genomes]
rs6950230	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6961358	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6961857	0.98[ASN][1000 genomes]
rs6963007	0.88[ASN][1000 genomes]
rs6971463	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6974968	0.81[ASN][1000 genomes]
rs6978101	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6978956	0.93[ASN][1000 genomes]
rs6979248	0.81[ASN][1000 genomes]
rs6979759	0.81[ASN][1000 genomes]
rs73678140	0.96[ASN][1000 genomes]
rs73678141	0.96[ASN][1000 genomes]
rs73678142	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73678143	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73678145	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73678147	0.98[ASN][1000 genomes]
rs73678149	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73680912	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs739889	0.87[ASN][1000 genomes]
rs739890	0.87[ASN][1000 genomes]
rs739891	0.87[ASN][1000 genomes]
rs7787685	0.97[ASN][1000 genomes]
rs7788250	0.96[ASN][1000 genomes]
rs7809961	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9692246	0.80[ASN][1000 genomes]
rs9692253	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv887596	chr7:10493399-10852392	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1067780	chr7:10649696-11329787	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv491695	chr7:10649696-11329787	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv1018905	chr7:10679889-10980691	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	nsv1019888	chr7:10712858-11496785	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv1029836	chr7:10713523-11492751	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv538730	chr7:10713523-11492751	Weak transcription Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
8	nsv532092	chr7:10731350-11414759	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
9	esv2752139	chr7:10798492-10954219	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
10	nsv887600	chr7:10807685-11090546	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
11	nsv1024171	chr7:10810444-11559156	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv949387	chr7:10815994-11281536	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
13	esv2752140	chr7:10817060-11029748	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
14	nsv824010	chr7:10819074-10820369	Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	esv998967	chr7:10819595-10820369	Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv824011	chr7:10819595-10820369	Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:10819400-10820200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:10819600-10820000	Active TSS	Spleen	Spleen
3	chr7:10819600-10821000	Active TSS	K562	blood

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