Variant report

Variant	rs72654668
Chromosome Location	chr4:79066261-79066262
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10000651	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs10002604	0.89[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs10003965	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs10004159	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs10005735	0.87[ASN][1000 genomes]
rs10007371	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs10018454	0.81[ASN][1000 genomes]
rs10023697	0.85[ASN][1000 genomes]
rs10025194	0.87[ASN][1000 genomes]
rs10025611	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs10025977	0.87[ASN][1000 genomes]
rs10026268	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs10028988	0.87[ASN][1000 genomes]
rs10030639	0.81[ASN][1000 genomes]
rs10033428	0.81[ASN][1000 genomes]
rs10213063	0.81[ASN][1000 genomes]
rs10213609	0.81[ASN][1000 genomes]
rs10518194	0.90[ASN][1000 genomes]
rs13133346	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs13136410	0.92[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs13144972	0.81[ASN][1000 genomes]
rs13150598	0.85[ASN][1000 genomes]
rs1317018	0.87[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs16997130	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs17418552	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17419053	0.93[ASN][1000 genomes]
rs17420118	0.97[ASN][1000 genomes]
rs17420328	0.97[ASN][1000 genomes]
rs1878437	0.87[ASN][1000 genomes]
rs2078481	0.87[ASN][1000 genomes]
rs28409486	0.84[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs28479828	0.81[ASN][1000 genomes]
rs28542863	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28597965	0.87[ASN][1000 genomes]
rs28635454	0.81[ASN][1000 genomes]
rs2867004	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs28671092	0.87[ASN][1000 genomes]
rs28677913	0.81[ASN][1000 genomes]
rs28707182	0.81[ASN][1000 genomes]
rs28750077	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs28822779	0.81[ASN][1000 genomes]
rs2903452	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs34552897	0.87[ASN][1000 genomes]
rs35374567	0.87[ASN][1000 genomes]
rs35967777	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4610363	0.81[ASN][1000 genomes]
rs4634250	0.81[ASN][1000 genomes]
rs55690666	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs56368720	0.87[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs58118093	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58969863	0.81[ASN][1000 genomes]
rs58970756	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs66631138	0.90[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6820400	0.81[ASN][1000 genomes]
rs6838483	0.81[ASN][1000 genomes]
rs6838661	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs6840121	0.81[ASN][1000 genomes]
rs6840357	0.87[ASN][1000 genomes]
rs6848061	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6857278	0.81[ASN][1000 genomes]
rs6857527	0.81[ASN][1000 genomes]
rs6858810	0.87[ASN][1000 genomes]
rs7666444	0.81[ASN][1000 genomes]
rs7670625	0.87[ASN][1000 genomes]
rs7673873	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7677432	0.87[ASN][1000 genomes]
rs7681238	0.87[ASN][1000 genomes]
rs7684543	0.81[ASN][1000 genomes]
rs7695979	0.87[ASN][1000 genomes]
rs7698326	0.85[ASN][1000 genomes]
rs7699120	0.87[ASN][1000 genomes]
rs9307335	0.81[ASN][1000 genomes]
rs9307336	0.81[ASN][1000 genomes]
rs9307337	0.81[ASN][1000 genomes]
rs9307338	0.81[ASN][1000 genomes]
rs9307339	0.81[ASN][1000 genomes]
rs9307340	0.81[ASN][1000 genomes]
rs9307352	0.85[ASN][1000 genomes]
rs9991356	0.81[ASN][1000 genomes]
rs9994298	0.81[ASN][1000 genomes]
rs9994422	0.81[ASN][1000 genomes]
rs9999763	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534024	chr4:78785189-79437403	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription 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	18 gene(s)	inside rSNPs	diseases
2	nsv1009633	chr4:78887573-79652236	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv520625	chr4:79002655-79071788	Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv525530	chr4:79024524-79266563	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv879502	chr4:79052851-79144309	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv1010782	chr4:79057839-79387207	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79054000-79068400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:79054000-79070400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:79057600-79068400	Weak transcription	Fetal Kidney	kidney
4	chr4:79060800-79067800	Weak transcription	HepG2	liver
5	chr4:79066000-79066600	Enhancers	H1 Cell Line	embryonic stem cell
6	chr4:79066000-79067000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr4:79066000-79067200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:79066200-79066600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:79066200-79067000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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