Variant report

Variant	rs10282397
Chromosome Location	chr7:11888728-11888729
allele	A/C
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:25)

rs_ID	r²[population]
rs10243925	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10259477	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13226381	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2355101	0.88[EUR][1000 genomes]
rs2355105	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2355106	0.81[CEU][hapmap]
rs2355110	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2355113	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2355114	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2883596	0.82[CEU][hapmap]
rs36083223	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6460847	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6460850	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6460851	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6942789	0.85[AMR][1000 genomes]
rs6943249	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6951563	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6958721	0.82[AFR][1000 genomes]
rs6960906	0.81[EUR][1000 genomes]
rs6961133	0.81[EUR][1000 genomes]
rs6964003	0.88[EUR][1000 genomes]
rs6966650	0.83[AFR][1000 genomes]
rs6978088	0.81[CEU][hapmap]
rs7807756	0.96[CEU][hapmap]
rs7807946	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv887614	chr7:11778424-12211198	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv830905	chr7:11793513-11941594	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv606203	chr7:11870711-11915630	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv887615	chr7:11870711-11938060	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv519418	chr7:11884682-11900479	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
7	nsv464368	chr7:11884682-11920546	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv606204	chr7:11884682-11920546	Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv887616	chr7:11884682-11931567	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv887617	chr7:11884682-11938060	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11886000-11890800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:11886400-11889000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr7:11886400-11889000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr7:11886400-11890400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr7:11886600-11889000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr7:11887000-11889000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr7:11887400-11890200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:11887400-11890400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr7:11888000-11889000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr7:11888200-11891400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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