Variant report

Variant	rs1364660
Chromosome Location	chr2:148538149-148538150
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:148505485..148507558-chr2:148536653..148539405,2	K562	blood:

Extended variants
information (count: 105 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1014064	0.96[CEU][hapmap];0.84[GIH][hapmap];0.90[TSI][hapmap];0.88[EUR][1000 genomes]
rs10460259	0.96[CEU][hapmap];0.83[GIH][hapmap];0.90[TSI][hapmap];0.80[EUR][1000 genomes]
rs10497024	0.96[CEU][hapmap];0.82[YRI][hapmap];0.87[EUR][1000 genomes]
rs10803523	0.91[CEU][hapmap];0.86[EUR][1000 genomes]
rs1128919	0.96[CEU][hapmap];0.89[GIH][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes]
rs11884013	0.94[EUR][1000 genomes]
rs11888152	0.96[CEU][hapmap];0.83[GIH][hapmap];0.90[TSI][hapmap]
rs11889608	0.90[EUR][1000 genomes]
rs11900506	0.92[CEU][hapmap];0.86[TSI][hapmap]
rs11901963	0.92[CEU][hapmap]
rs11904758	0.87[EUR][1000 genomes]
rs12053113	0.85[EUR][1000 genomes]
rs12463798	0.92[CEU][hapmap]
rs12464617	0.90[EUR][1000 genomes]
rs12469504	0.81[EUR][1000 genomes]
rs12469939	0.81[EUR][1000 genomes]
rs12472058	0.94[EUR][1000 genomes]
rs12475399	0.94[EUR][1000 genomes]
rs12479193	0.94[EUR][1000 genomes]
rs12987286	0.86[ASW][hapmap];0.96[CEU][hapmap];0.97[GIH][hapmap];0.91[MKK][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes]
rs12989596	0.87[EUR][1000 genomes]
rs12990959	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs12997065	0.89[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs12998729	0.96[CEU][hapmap];0.97[GIH][hapmap];0.93[TSI][hapmap];0.88[EUR][1000 genomes]
rs13000597	0.86[EUR][1000 genomes]
rs13004041	0.81[EUR][1000 genomes]
rs13004451	0.88[EUR][1000 genomes]
rs13005423	0.93[EUR][1000 genomes]
rs13006184	0.81[EUR][1000 genomes]
rs13008497	0.96[CEU][hapmap];0.82[YRI][hapmap];0.85[EUR][1000 genomes]
rs13013743	0.90[EUR][1000 genomes]
rs13013867	0.90[EUR][1000 genomes]
rs13014904	0.90[EUR][1000 genomes]
rs13014926	0.82[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs13016083	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13017754	0.90[EUR][1000 genomes]
rs13019386	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13019809	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs13022319	0.85[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs13025219	0.88[EUR][1000 genomes]
rs13025589	0.90[EUR][1000 genomes]
rs13025701	0.94[EUR][1000 genomes]
rs13026220	0.90[EUR][1000 genomes]
rs13026650	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs13027200	0.81[EUR][1000 genomes]
rs13027706	0.95[CEU][hapmap];0.80[EUR][1000 genomes]
rs13028411	0.86[EUR][1000 genomes]
rs13031064	0.80[EUR][1000 genomes]
rs13033696	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs13034494	0.88[EUR][1000 genomes]
rs13034561	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1345994	0.81[EUR][1000 genomes]
rs1364658	0.96[CEU][hapmap];0.82[YRI][hapmap];0.88[EUR][1000 genomes]
rs1424944	0.95[CEU][hapmap];0.90[EUR][1000 genomes]
rs1424946	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1424949	0.94[EUR][1000 genomes]
rs1424952	0.81[ASN][1000 genomes]
rs1424954	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs1469210	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs1531032	0.96[CEU][hapmap];0.84[GIH][hapmap];0.90[TSI][hapmap];0.80[EUR][1000 genomes]
rs16827722	0.83[TSI][hapmap]
rs16855486	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1863152	0.92[CEU][hapmap];0.88[TSI][hapmap];0.94[EUR][1000 genomes]
rs1863153	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs1895693	0.86[EUR][1000 genomes]
rs1991169	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs2113793	0.96[CEU][hapmap]
rs2161983	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs2161984	0.96[CEU][hapmap]
rs2161985	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2288190	0.80[CEU][hapmap]
rs2303392	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs2307394	0.96[CEU][hapmap];0.84[GIH][hapmap];0.90[TSI][hapmap];0.80[EUR][1000 genomes]
rs34005843	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34539489	0.80[EUR][1000 genomes]
rs35370215	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3764955	0.96[CEU][hapmap];0.82[YRI][hapmap];0.86[EUR][1000 genomes]
rs3768687	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs3768689	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs3926960	0.81[EUR][1000 genomes]
rs4972272	0.94[EUR][1000 genomes]
rs4972316	0.82[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs4972356	0.90[EUR][1000 genomes]
rs4972357	0.87[EUR][1000 genomes]
rs57679331	0.80[EUR][1000 genomes]
rs6430241	0.94[EUR][1000 genomes]
rs6430242	0.94[EUR][1000 genomes]
rs6711673	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs6729465	0.80[EUR][1000 genomes]
rs6729997	0.86[EUR][1000 genomes]
rs6734998	0.92[CEU][hapmap];0.88[TSI][hapmap];0.94[EUR][1000 genomes]
rs6760703	0.87[EUR][1000 genomes]
rs723681	0.96[CEU][hapmap];0.82[YRI][hapmap];0.86[EUR][1000 genomes]
rs7559714	0.87[EUR][1000 genomes]
rs7559925	0.88[EUR][1000 genomes]
rs7594075	0.80[EUR][1000 genomes]
rs7600869	0.94[EUR][1000 genomes]
rs929939	0.87[CEU][hapmap];0.83[GIH][hapmap];0.90[TSI][hapmap];0.86[EUR][1000 genomes]
rs9679427	0.94[EUR][1000 genomes]
rs987122	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875275	chr2:148166428-148711242	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv916286	chr2:148438001-148977722	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv529388	chr2:148471340-148934846	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	esv3392562	chr2:148476961-148843061	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	esv1842822	chr2:148505544-148542682	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1364660	DYNLL1	trans	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148535000-148540400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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