Variant report

Variant	rs61037288
Chromosome Location	chr7:7504879-7504880
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10226811	0.92[ASN][1000 genomes]
rs10229355	0.90[ASN][1000 genomes]
rs10247676	0.90[ASN][1000 genomes]
rs10250746	0.82[ASN][1000 genomes]
rs10250756	0.82[ASN][1000 genomes]
rs10250860	0.82[ASN][1000 genomes]
rs10255190	0.82[ASN][1000 genomes]
rs10255201	0.84[ASN][1000 genomes]
rs1029571	0.84[ASN][1000 genomes]
rs10486160	0.84[ASN][1000 genomes]
rs10486163	0.84[ASN][1000 genomes]
rs10486165	0.86[ASN][1000 genomes]
rs10486166	0.92[ASN][1000 genomes]
rs10486168	0.90[ASN][1000 genomes]
rs10486171	0.92[ASN][1000 genomes]
rs10486173	0.81[ASN][1000 genomes]
rs10486175	0.89[ASN][1000 genomes]
rs12666561	0.82[ASN][1000 genomes]
rs16878046	0.84[ASN][1000 genomes]
rs16878062	0.86[ASN][1000 genomes]
rs17151541	0.82[ASN][1000 genomes]
rs17151547	0.82[ASN][1000 genomes]
rs17167601	0.81[ASN][1000 genomes]
rs17167625	0.84[ASN][1000 genomes]
rs17168096	0.92[ASN][1000 genomes]
rs17168127	0.92[ASN][1000 genomes]
rs17168144	0.90[ASN][1000 genomes]
rs17168145	0.90[ASN][1000 genomes]
rs17168152	0.81[ASN][1000 genomes]
rs17168215	0.92[ASN][1000 genomes]
rs17168295	0.85[ASN][1000 genomes]
rs17168350	0.81[ASN][1000 genomes]
rs17168365	0.81[ASN][1000 genomes]
rs17168367	0.82[ASN][1000 genomes]
rs17168368	0.81[ASN][1000 genomes]
rs17168369	0.81[ASN][1000 genomes]
rs17510752	0.82[ASN][1000 genomes]
rs2109772	0.82[ASN][1000 genomes]
rs2286839	0.84[ASN][1000 genomes]
rs4320465	0.87[ASN][1000 genomes]
rs4543457	0.92[ASN][1000 genomes]
rs55798422	0.92[ASN][1000 genomes]
rs55827101	0.92[ASN][1000 genomes]
rs55841745	0.81[ASN][1000 genomes]
rs55924331	0.84[ASN][1000 genomes]
rs55980077	0.92[ASN][1000 genomes]
rs56022797	0.92[ASN][1000 genomes]
rs56084871	0.92[ASN][1000 genomes]
rs56103225	0.80[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs56177814	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs56330916	0.92[ASN][1000 genomes]
rs57521604	0.90[ASN][1000 genomes]
rs58324484	0.82[ASN][1000 genomes]
rs60314248	0.84[ASN][1000 genomes]
rs60668247	0.92[ASN][1000 genomes]
rs60977515	0.92[ASN][1000 genomes]
rs61221982	0.92[ASN][1000 genomes]
rs61543470	0.90[ASN][1000 genomes]
rs6945969	0.92[ASN][1000 genomes]
rs6948300	0.87[ASN][1000 genomes]
rs6948753	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6949534	0.84[ASN][1000 genomes]
rs6955328	0.92[ASN][1000 genomes]
rs6962455	0.92[ASN][1000 genomes]
rs6963106	0.92[ASN][1000 genomes]
rs6964749	0.92[ASN][1000 genomes]
rs6965546	0.92[ASN][1000 genomes]
rs6968394	0.82[ASN][1000 genomes]
rs6971367	0.92[ASN][1000 genomes]
rs6971414	0.84[ASN][1000 genomes]
rs6971456	0.90[ASN][1000 genomes]
rs6972142	0.92[ASN][1000 genomes]
rs6975571	0.92[ASN][1000 genomes]
rs73346330	0.92[ASN][1000 genomes]
rs7459128	0.84[ASN][1000 genomes]
rs7778212	0.84[ASN][1000 genomes]
rs7780426	0.92[ASN][1000 genomes]
rs7789255	0.84[ASN][1000 genomes]
rs7798119	0.81[ASN][1000 genomes]
rs929378	0.84[ASN][1000 genomes]
rs972766	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023133	chr7:6854098-7516700	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv869091	chr7:6927461-7567820	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv949293	chr7:6990891-7711883	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
4	nsv1030246	chr7:7053923-7569633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv1019498	chr7:7053923-7668373	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
6	nsv538721	chr7:7053923-7668373	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription 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 miRNA target site	54 gene(s)	inside rSNPs	diseases
7	nsv1026758	chr7:7187491-8075259	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
8	nsv887470	chr7:7310023-7655094	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv887472	chr7:7405069-7680697	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
10	nsv606042	chr7:7427535-7876466	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
11	nsv606043	chr7:7473563-7571420	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv887473	chr7:7497676-7604913	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7490400-7513800	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr7:7501200-7518200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:7501400-7511600	Weak transcription	Pancreas	Pancrea
4	chr7:7503000-7512000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr7:7504000-7505200	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr7:7504600-7505000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr7:7504600-7505000	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr7:7504600-7505200	Active TSS	H9 Cell Line	embryonic stem cell
9	chr7:7504800-7505000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell

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