Variant report

Variant	rs2412665
Chromosome Location	chr4:56472979-56472980
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:56468709..56470290-chr4:56471936..56473680,2	K562	blood:
2	chr4:56471770..56474121-chr4:56475653..56477265,2	K562	blood:
3	chr4:56472523..56475869-chr4:56480434..56484043,4	K562	blood:
4	chr4:56472621..56475219-chr4:56475225..56477153,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10000512	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs10011089	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs10011801	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs10017749	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10018932	0.96[ASN][1000 genomes]
rs10026315	0.98[ASN][1000 genomes]
rs10026676	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10029142	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13434995	0.89[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs17725110	1.00[ASN][1000 genomes]
rs17725163	0.98[ASN][1000 genomes]
rs17781708	0.98[ASN][1000 genomes]
rs1873090	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs1873091	1.00[ASN][1000 genomes]
rs2412666	1.00[ASN][1000 genomes]
rs28416150	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs28435401	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs28451532	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs28473211	0.98[ASN][1000 genomes]
rs28564902	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28708716	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28713371	0.95[ASN][1000 genomes]
rs28756087	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs3805383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3805385	0.98[ASN][1000 genomes]
rs3805387	0.98[ASN][1000 genomes]
rs3805388	0.98[ASN][1000 genomes]
rs3805389	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55849318	0.98[ASN][1000 genomes]
rs56288855	0.96[ASN][1000 genomes]
rs57178140	0.98[ASN][1000 genomes]
rs59571323	0.95[ASN][1000 genomes]
rs62308665	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62308667	0.98[ASN][1000 genomes]
rs62308708	0.88[ASN][1000 genomes]
rs62310884	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73236165	0.98[ASN][1000 genomes]
rs9790448	0.89[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs9996936	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][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	esv3328582	chr4:56164136-56486156	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	esv2755990	chr4:56317136-57143037	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
3	nsv10496	chr4:56336946-56841137	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv998179	chr4:56425126-56694339	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv932636	chr4:56438618-56667329	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56464200-56475800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:56465400-56479400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:56465600-56476000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:56469800-56481200	Weak transcription	Esophagus	oesophagus
5	chr4:56470400-56478800	Strong transcription	K562	blood
6	chr4:56472400-56476600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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