Variant report

Variant	rs10255778
Chromosome Location	chr7:146673289-146673290
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10081175	0.85[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap]
rs10081247	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10228803	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10238991	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10242195	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10243212	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10251563	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10267864	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10268255	1.00[JPT][hapmap]
rs10500168	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11773694	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11982298	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11982450	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11983087	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12216586	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12690893	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12703847	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12703848	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12703858	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12703863	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12703867	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12703869	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13224666	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13233800	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17133799	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17170293	1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap]
rs1916934	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1916939	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1916946	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4130001	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7792455	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs940455	1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv1027561	chr7:146308783-146762872	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv531440	chr7:146399958-146691013	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv465191	chr7:146406379-146759900	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv608941	chr7:146406379-146759900	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv916943	chr7:146445929-146682066	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv522917	chr7:146446767-146694441	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv933923	chr7:146450952-146690007	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv534580	chr7:146451347-146730531	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv1021251	chr7:146522341-146802125	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv497792	chr7:146526101-146734852	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv1019300	chr7:146652162-146680329	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv531442	chr7:146669919-146755110	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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