Variant report

Variant	rs4768891
Chromosome Location	chr12:50754357-50754358
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	chr12:50753415..50756323-chr12:50757953..50759576,2	K562	blood:

Variant related genes	Relation type
ENSG00000244266	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10467106	0.89[EUR][1000 genomes]
rs10506292	0.85[EUR][1000 genomes]
rs10783349	0.90[AFR][1000 genomes]
rs10783350	0.90[AFR][1000 genomes]
rs10783352	0.86[EUR][1000 genomes]
rs10783353	0.91[EUR][1000 genomes]
rs10876018	0.86[AFR][1000 genomes]
rs10876023	0.90[EUR][1000 genomes]
rs10876027	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10876028	0.93[EUR][1000 genomes]
rs11169379	0.95[AFR][1000 genomes]
rs11169386	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs11169390	0.91[EUR][1000 genomes]
rs11169391	0.90[EUR][1000 genomes]
rs11169395	0.92[EUR][1000 genomes]
rs12299669	0.87[EUR][1000 genomes]
rs12299758	0.91[EUR][1000 genomes]
rs12303082	0.93[EUR][1000 genomes]
rs12422417	0.92[EUR][1000 genomes]
rs12582180	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12814094	0.92[EUR][1000 genomes]
rs12821504	0.81[AFR][1000 genomes]
rs36017775	0.84[EUR][1000 genomes]
rs4348979	0.93[EUR][1000 genomes]
rs4421818	0.91[EUR][1000 genomes]
rs4445717	0.86[EUR][1000 genomes]
rs4768855	0.90[EUR][1000 genomes]
rs4768951	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6580736	0.82[AFR][1000 genomes]
rs6580740	0.90[AFR][1000 genomes]
rs6580743	0.91[EUR][1000 genomes]
rs7295847	0.85[EUR][1000 genomes]
rs7296291	0.85[EUR][1000 genomes]
rs7302363	0.92[EUR][1000 genomes]
rs7312252	0.85[EUR][1000 genomes]
rs7485486	0.90[AFR][1000 genomes]
rs7489214	0.95[AFR][1000 genomes]
rs7971374	0.84[EUR][1000 genomes]
rs7972824	0.92[EUR][1000 genomes]
rs7973243	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7976270	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9668187	0.90[EUR][1000 genomes]
rs9739363	0.93[EUR][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	nsv899075	chr12:50594947-50835060	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
2	esv2761738	chr12:50627292-50836427	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
3	nsv1035796	chr12:50634342-50784312	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv1053667	chr12:50679039-50801752	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	nsv1054480	chr12:50691039-50859665	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
6	nsv1041563	chr12:50705715-50861699	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv1049665	chr12:50705715-50871542	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4768891	DIP2B	Cis_1M	lymphoblastoid	RTeQTL
rs4768891	CERS5	cis	Nerve Tibial	GTEx

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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