Variant report

Variant	rs10443242
Chromosome Location	chr1:58526235-58526236
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:31)

rs_ID	r²[population]
rs10443219	1.00[CEU][hapmap];0.82[CHB][hapmap];0.97[GIH][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10443244	0.97[ASN][1000 genomes]
rs10443245	1.00[CEU][hapmap];0.82[CHB][hapmap];0.88[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10443246	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10443247	1.00[ASN][1000 genomes]
rs10889081	1.00[CEU][hapmap];0.82[CHB][hapmap];0.97[GIH][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10889082	1.00[ASN][1000 genomes]
rs11207162	0.93[CHB][hapmap];0.85[JPT][hapmap]
rs11207165	1.00[CEU][hapmap];0.93[CHB][hapmap];0.81[JPT][hapmap];0.86[YRI][hapmap]
rs11207166	1.00[CEU][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap]
rs12124142	0.82[CHB][hapmap];0.99[ASN][1000 genomes]
rs12563473	1.00[CEU][hapmap];0.82[CHB][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1408925	1.00[CEU][hapmap];0.82[CHB][hapmap];0.97[GIH][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17116775	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17116802	0.82[CHB][hapmap];1.00[ASN][1000 genomes]
rs2025616	1.00[CEU][hapmap];0.82[CHB][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2806403	0.88[GIH][hapmap];0.92[TSI][hapmap];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2808814	1.00[CEU][hapmap];0.82[CHB][hapmap];0.94[GIH][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2808822	1.00[CEU][hapmap];0.82[CHB][hapmap];0.94[GIH][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34678610	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3753508	1.00[ASN][1000 genomes]
rs3753509	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57920068	0.99[ASN][1000 genomes]
rs58537714	1.00[ASN][1000 genomes]
rs6587800	0.95[ASN][1000 genomes]
rs6657936	0.82[CHB][hapmap];0.87[GIH][hapmap];1.00[ASN][1000 genomes]
rs6677854	0.87[CHB][hapmap];0.99[ASN][1000 genomes]
rs7515158	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7516066	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[YRI][hapmap];0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7527995	0.95[ASN][1000 genomes]
rs7548316	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015057	chr1:57976993-58793962	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv530017	chr1:58002290-58669736	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv431379	chr1:58224212-58802608	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv527673	chr1:58526235-58531627	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58524600-58526800	Enhancers	Fetal Brain Male	brain
2	chr1:58525200-58526600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:58525200-58526800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr1:58525400-58526400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:58525400-58526800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr1:58525600-58526600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:58525600-58526800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:58525800-58526600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr1:58525800-58529800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr1:58525800-58531600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr1:58526000-58526600	Weak transcription	Fetal Brain Female	brain
12	chr1:58526000-58530000	Weak transcription	H1 Cell Line	embryonic stem cell

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