Variant report

Variant	rs7904615
Chromosome Location	chr10:1697676-1697677
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11250698	0.80[AMR][1000 genomes]
rs11250702	0.86[CEU][hapmap];0.96[GIH][hapmap];0.91[MEX][hapmap];0.88[MKK][hapmap];0.81[AMR][1000 genomes]
rs11250703	0.86[CEU][hapmap];0.85[AMR][1000 genomes]
rs11250714	0.95[CEU][hapmap];1.00[GIH][hapmap];0.87[TSI][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12767490	0.81[AMR][1000 genomes]
rs17221916	0.86[CEU][hapmap];0.85[AMR][1000 genomes]
rs3750685	1.00[CEU][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4880524	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4880890	0.82[CEU][hapmap];0.92[GIH][hapmap];0.82[MEX][hapmap]
rs4880891	0.82[CEU][hapmap]
rs4880894	0.80[CEU][hapmap]
rs4880899	0.85[AMR][1000 genomes]
rs4880901	0.87[CEU][hapmap];0.87[AMR][1000 genomes]
rs4880903	0.95[CEU][hapmap];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4880904	0.95[CEU][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.87[TSI][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7071633	0.95[CEU][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7078581	0.87[CEU][hapmap];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7078890	0.94[CEU][hapmap];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7901958	0.86[CEU][hapmap];0.85[AMR][1000 genomes]
rs7918604	0.91[CEU][hapmap];0.86[AMR][1000 genomes];0.83[EUR][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	nsv530117	chr10:945438-1729634	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv817532	chr10:964660-1885945	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1041498	chr10:1117200-1760190	Genic enhancers Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv1046041	chr10:1195214-2189155	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
5	nsv1037054	chr10:1232041-1865296	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv540413	chr10:1232041-1865296	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv549769	chr10:1244020-1764966	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv549786	chr10:1293100-1904598	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv1054555	chr10:1558145-1965145	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1052401	chr10:1582012-1964762	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv540417	chr10:1582012-1964762	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv894738	chr10:1613026-1791836	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	nsv549796	chr10:1665211-1747923	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv1043576	chr10:1667645-1901205	Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv894741	chr10:1669880-1736049	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:1689200-1700000	Weak transcription	Brain Substantia Nigra	brain
2	chr10:1693600-1698400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:1695200-1700600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr10:1695200-1700800	Weak transcription	Fetal Brain Female	brain
5	chr10:1695200-1704000	Weak transcription	Spleen	Spleen
6	chr10:1695400-1712000	Weak transcription	Gastric	stomach
7	chr10:1696800-1698000	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr10:1697000-1697800	Enhancers	Fetal Intestine Large	intestine
9	chr10:1697000-1697800	Enhancers	GM12878-XiMat	blood
10	chr10:1697200-1698000	Enhancers	Liver	Liver
11	chr10:1697200-1698000	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr10:1697400-1700800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr10:1697600-1699800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr10:1697600-1700200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr10:1697600-1700600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr10:1697600-1702200	Weak transcription	Pancreas	Pancrea

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