Variant report

Variant	rs1830612
Chromosome Location	chr10:37999883-37999884
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10740949	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10764142	0.93[ASN][1000 genomes]
rs10764143	1.00[ASN][1000 genomes]
rs10764144	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10827815	0.97[ASN][1000 genomes]
rs10827818	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10827819	0.91[ASN][1000 genomes]
rs11011323	0.97[ASN][1000 genomes]
rs11011324	0.96[ASN][1000 genomes]
rs11011325	0.97[ASN][1000 genomes]
rs11011339	1.00[ASN][1000 genomes]
rs11011341	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11011346	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1148287	1.00[CEU][hapmap]
rs11597720	1.00[ASN][1000 genomes]
rs1208645	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs1208683	0.89[CEU][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs1208695	0.80[EUR][1000 genomes]
rs1208770	0.86[EUR][1000 genomes]
rs1208779	0.82[EUR][1000 genomes]
rs1212108	1.00[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs12357413	0.97[ASN][1000 genomes]
rs12570943	0.93[ASN][1000 genomes]
rs12776092	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12783272	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1742235	0.86[EUR][1000 genomes]
rs2753877	0.85[EUR][1000 genomes]
rs34185758	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4934898	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61858629	0.92[ASN][1000 genomes]
rs734512	1.00[ASN][1000 genomes]
rs7476802	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895030	chr10:37715737-38674609	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking 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 target site	53 gene(s)	inside rSNPs	diseases
2	nsv1045684	chr10:37765361-38426204	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv540564	chr10:37765361-38426204	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1040704	chr10:37940024-38451917	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS 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 target site	40 gene(s)	inside rSNPs	diseases
5	esv1794823	chr10:37961177-38002067	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv975072	chr10:37990724-38017623	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv975812	chr10:37990724-38084639	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:37999000-38002200	Enhancers	HSMMtube	muscle
2	chr10:37999400-38002200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:37999600-38000000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr10:37999600-38002000	Enhancers	HSMM	muscle
5	chr10:37999800-38000000	Enhancers	NHLF	lung
6	chr10:37999800-38000200	Enhancers	A549	lung
7	chr10:37999800-38000400	Enhancers	Lung	lung
8	chr10:37999800-38002200	Enhancers	Left Ventricle	heart
9	chr10:37999800-38002200	Enhancers	Right Atrium	heart
10	chr10:37999800-38002600	Enhancers	Right Ventricle	heart

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